Other products from "TELA BIO, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00856072005289 R20252-1020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
2 00856072005197 R20253-1122G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
3 00856072005142 R20243-1122P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
4 00856072005135 R20243-1018P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
5 00856072005111 R20153-2020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
6 00856072005074 R20143-2020P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
7 00856072005043 R20143-0416P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
8 00856072005036 R20252-1122G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
9 00856072005029 R20252-0815G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
10 00856072005012 R20152-2020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
11 00856072005005 R20152-1620G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. FTM,FTL Mesh, Surgical,Mesh, Surgical, Polymeric 2 OviTex® PRS
12 00856072005562 F10333-0822T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
13 00856072005555 F10331-1012T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
14 10856072005088 F10069-1822 F10069-1822 TELAMax 1S is a sterile bioscaffold composed of ovine (sheep) derived extracellu TELAMax 1S is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene. The device consists of two sides: a textured and smooth side. The textured side of the device, indicated with blue polypropylene, provides a surface conducive for tissue ingrowth. The smooth side of the device, containing clear polypropylene, provides a surface designed to minimize tissue attachment. TELAMax 1S will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. TELAMax 1S is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient's requirements. FTM Mesh, Surgical 2 TELAMax 1S
15 00856072005654 F10345-0610T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
16 00856072005647 F10345-0608T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
17 00856072005630 F10340-0608T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
18 00856072005623 F10339-1012T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
19 00856072005616 F10338-0610T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
20 00856072005586 F10335-1012T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
21 00856072005579 F10334-0822T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
22 00856072005548 F10330-0610T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
23 00856072005531 F10329-0610T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
24 00856072005272 F10269-1015T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
25 00810055070923 F10342-1017T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
26 00810055070916 F10341-1016T The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. FZX Guide, Surgical, Instrument 1 OviTex®
27 10856072005132 F10068-0408 F10068-0408 TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene. TELAMax will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. TELAMax is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient's requirements. FTM Mesh, Surgical 2 TELAMax
28 10856072005026 F10068-1010 F10068-1010 TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene. TELAMax will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. TELAMax is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient's requirements. FTM Mesh, Surgical 2 TELAMax
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No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
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10 00868047000380 31056 FlexBand 0.7 x 16 Strip FlexBand ARTELON
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12 00868047000366 31054 FlexBand 0.5 x 16 Strip FlexBand ARTELON
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14 00868047000342 31052 FlexBand 0.3 x 16 Strip FlexBand ARTELON
15 00868047000335 31051 FlexBand 0.3 x 8 Strip FlexBand ARTELON
16 00868047000328 31049 FlexBand 6 x 9 Mesh FlexBand ARTELON
17 00868047000311 31050 FlexBand 3 x 4 Mesh FlexBand ARTELON
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19 00860002305141 XI-S+ XI0909C-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
20 00860002305134 XI-S+ XI1014B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
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24 00860000875943 PTM2025 DuraSorb Monofilament Mesh SURGICAL INNOVATION ASSOCIATES, INC.
25 00860000875929 PTM0616 DuraSorb Monofilament Mesh SURGICAL INNOVATION ASSOCIATES, INC.
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27 00859389005119 CMCV-009-XXL The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
28 00859389005072 CMCV-009-XLG The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
29 00859389005065 CMCV-009-LRG The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
30 00859389005034 CMCV-009-MED The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
31 00859389005027 CMCV-009-SML The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. CanGaroo Envelope AZIYO BIOLOGICS, INC.
32 00856072005142 R20243-1122P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
33 00857072005057 BLM-100-01-1020 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
34 00857072005040 BLM-100-01-1016 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
35 00857072005033 BLM-100-01-0816 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
36 00857072005026 BLM-100-01-1010 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
37 00857072005019 BLM-100-01-0808 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
38 00857072005002 BLM-100-01-0608 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
39 00856072005289 R20252-1020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
40 00856072005289 R20252-1020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
41 00856072005197 R20253-1122G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
42 00856072005197 R20253-1122G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
43 00856072005142 R20243-1122P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
44 00856072005135 R20243-1018P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
45 00856072005135 R20243-1018P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
46 00856072005111 R20153-2020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
47 00856072005111 R20153-2020G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
48 00856072005104 R20153-1620G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
49 00856072005104 R20153-1620G OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.
50 00856072005074 R20143-2020P OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. OviTex® PRS TELA BIO, INC.