Other products from "STELLEN MEDICAL, LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00855638007194 PC The Skin Graft Mesher is a surigical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
2 00855638007187 2:1 The Skin Graft Mesher is a surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
3 00855638007170 3:1 The Skin Graft Mesher is a surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
4 00855638007163 4:1 The Skin Graft Mesher is surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
5 00855638007156 6:1 The Skin Graft Mesher is a surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
6 00855638007149 1:1 The Skin Graft Mesher is a surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
7 00855638007101 GPC-0025 GPC-0025 GlucanPro Cream is intended to be used as an aid in the management of superficia GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic U GlucanPro
8 00855638007088 GPC-0085 GPC-0085 GlucanPro Cream is intended to be used as an aid in the management of superficia GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers, venous, diabetic and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic U GlucanPro
9 00855638007064 GPC3-0180 GPC3-0180 GlucanPro Cream is intended to be used as an aid in the management of superficia GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic U GlucanPro 3000
10 00855638007040 GPC3-0035 GPC3-0035 GlucanPro Cream is intended to be used as an aid in the management of superficia GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic GlucanPro 3000
11 00855638007125 GEL-6505 GEL-6505 : NovaGel is indicated for use as a scar management dressing on old and new hyp : NovaGel is indicated for use as a scar management dressing on old and new hypertrophic or keloid scars. MDA Elastomer, Silicone, For Scar Management Nova Gel
12 00855638007033 3102-2152 Acellular dermal matrix FTM Mesh, Surgical 2 ProLayer Xenograft
13 00855638007026 3102-2147 Acellular Dermal Matrix FTM Mesh, Surgical 2 ProLayer Xenograft
14 00855638007002 3102-2125 Acellular Dermal Matrix FTM Mesh, Surgical 2 ProLayer Xenograft
15 M070PR05101 PR-0510 PR-0510 Multi-purpose implantable surgical mesh, collagen, bioabsorbable-for use in proc Multi-purpose implantable surgical mesh, collagen, bioabsorbable-for use in procedures such as achilles repair, rotator cuff and ligaments. FTM Mesh, Surgical 2 Proformix
16 M070PR04071 PR-0407 PR-04074 Multi-purpose implantable surgical mesh, collagen, bioabsorbable-for use in proc Multi-purpose implantable surgical mesh, collagen, bioabsorbable-for use in procedures such as achilles repair, rotator cuff and ligaments. FTM Mesh, Surgical 2 Proformix
17 M070PR02051 PR-0205 PR-0205 Multi-purpose Implantable surgical mesh, collagen, bioabsorable- for use in proc Multi-purpose Implantable surgical mesh, collagen, bioabsorable- for use in procedure such as achilles repair, rotator cuff and ligments. FTM Mesh, Surgical 2 Proformix
Other products with the same Product Code "FTM"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00868623000360 XI-S+ XI0404-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
2 00868623000353 XI-S+ XI0203-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
3 00868623000346 XI-S+ XI0710-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
4 00868623000339 XI-S+ XI0808-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
5 00868623000322 XI-S+ XI0508-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
6 00868623000315 XI-S+ XI0615-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
7 00868623000308 XI-S+ XI0606-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
8 00860002305141 XI-S+ XI0909C-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
9 00860002305134 XI-S+ XI1014B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
10 00860002305127 XI-S+ XI1014A-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
11 00860002305110 XI-S+ XI1116B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
12 00860002305103 XI-S+ XI1116A-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
13 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.
14 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.
15 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.
16 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.
17 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.
18 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.
19 00857072005057 BLM-100-01-1020 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
20 00857072005040 BLM-100-01-1016 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
21 00857072005033 BLM-100-01-0816 Biologic Matrix MIROMESH® REPRISE BIOMEDICAL, INC.
22 00857072005026 BLM-100-01-1010 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
23 00857072005019 BLM-100-01-0808 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
24 00857072005002 BLM-100-01-0608 Biologic Matrix MiroFlex® REPRISE BIOMEDICAL, INC.
25 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.
26 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.
27 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.
28 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.
29 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.
30 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.
31 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. OviTex® PRS TELA BIO, INC.
32 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. OviTex® PRS TELA BIO, INC.
33 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. OviTex® PRS TELA BIO, INC.
34 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. OviTex® PRS TELA BIO, INC.
35 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. OviTex® PRS TELA BIO, INC.
36 00855638007033 3102-2152 Acellular dermal matrix ProLayer Xenograft STELLEN MEDICAL, LLC
37 00855638007026 3102-2147 Acellular Dermal Matrix ProLayer Xenograft STELLEN MEDICAL, LLC
38 00855638007019 3102-2144 Acellular Dermal Matrix ProLayer Xenograft STELLEN MEDICAL, LLC
39 00855638007002 3102-2125 Acellular Dermal Matrix ProLayer Xenograft STELLEN MEDICAL, LLC
40 00854501006036 2999-3 Rotation Medical Reconstituted Collagen Scaffold - Mini-Open, Large SMITH & NEPHEW, INC.
41 00854501006029 2999-2 Rotation Medical Reconstituted Collagen Scaffold - Mini-Open, Medium SMITH & NEPHEW, INC.
42 00840663106349 e10P16 e10P16 XenoSure Biologic Patch, 10cm x 16cm, eIFU XenoSure Biologic Patch LEMAITRE VASCULAR, INC.
43 00840663106332 e8P14 e8P14 XenoSure Biologic Patch, 8cm x 14cm, eIFU XenoSure Biologic Patch LEMAITRE VASCULAR, INC.
44 00840663106325 e4P6 e4P6 XenoSure Biologic Patch, 4cm x 6cm, eIFU XenoSure Biologic Patch LEMAITRE VASCULAR, INC.
45 00840663106318 e4P4 e4P4 XenoSure Biologic Patch, 4cm x 4cm, eIFU XenoSure Biologic Patch LEMAITRE VASCULAR, INC.
46 00840663106301 e2P9 e2P9 XenoSure Biologic Patch, 2cm x 9cm, eIFU XenoSure Biologic Patch LEMAITRE VASCULAR, INC.
47 00840663106295 e0.8P8 e0.8P8 XenoSure Biologic Patch, 0.8cm x 8cm, eIFU XenoSure Biologic Patch LEMAITRE VASCULAR, INC.
48 00840663106288 e1P6 e1P6 XenoSure Biologic Patch, 1cm x 6cm XenoSure Biologic Patch LEMAITRE VASCULAR, INC.
49 00840663106097 1BV10 XenoSure Biologic Patch, 1cmx10cm XenoSure Biologic Patch LEMAITRE VASCULAR, INC.
50 00840663106356 e1P14 e1P14 XenoSure Biologic Patch, 1cm x 14cm, eIFU XenoSure Biologic Patch LEMAITRE VASCULAR, INC.