Geistlich Derma-Gide™ 500476
Geistlich Derma-Gide™ 500476 is a device classified as Unclassified made by Geistlich Pharma AG, cleared under FDA 510(k) K182838 on 8 Nov 2018 and listed in FDA GUDID since 31 Jan 2019 (UDI-DI 07610221013180), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07610221013180 | Date31 Jan 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK182838 | Date8 Nov 2018 | StatusActive |
Official records
- AccessGUDID record 07610221013180
- FDA 510(k) database K182838
Across registries
- FDA 510(k) K182838 decided 8 Nov 2018 Active
- FDA GUDID UDI-DI 07610221013180 listed 31 Jan 2019 Listed
Timeline
- Cleared FDA 510(k) K182838
- Listed FDA GUDID 07610221013180
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Geistlich Derma-Gide™
- Generic name
- Animal-derived wound matrix dressing
- Model / reference
- 500476
- Primary DI / UDI-DI
- 07610221013180
- 510(k) Number
- FDA product code
- KGN
- GMDN term
- Animal-derived wound matrix dressing
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 10 Millimeter
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