Duns Number:125850144
Device Description: Kit containing:R630 Pineyro Arch™ Ti 1R631 Pineyro Arch™ Ti 2R632 Pineyro Arch™ Ti 3R633 P Kit containing:R630 Pineyro Arch™ Ti 1R631 Pineyro Arch™ Ti 2R632 Pineyro Arch™ Ti 3R633 Pineyro Arch™ Ti 4
Catalog Number
R931
Brand Name
PDT, Inc.
Version/Model Number
R931 Pineyro Arch™ Kit (Instruments Only)
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
ECP
Product Code Name
Instrument, Ligature Tucking, Orthodontic
Public Device Record Key
e086602c-6697-4dde-9108-c02f6554d9d8
Public Version Date
May 10, 2021
Public Version Number
1
DI Record Publish Date
April 30, 2021
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 248 |