ProGrip ADG1510
ProGrip ADG1510 is a Class II device made by Sofradim Production, cleared under FDA 510(k) K253956 on 21 May 2026 and listed in FDA GUDID since 19 Jun 2026 (UDI-DI 10884521851672), 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 | Number10884521851672 | Date19 Jun 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK253956 | Date21 May 2026 | StatusActive |
Official records
- AccessGUDID record 10884521851672
- FDA 510(k) database K253956
Across registries
- FDA 510(k) K253956 decided 21 May 2026 Active
- FDA GUDID UDI-DI 10884521851672 listed 19 Jun 2026 Listed
Timeline
- Cleared FDA 510(k) K253956
- Listed FDA GUDID 10884521851672
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ProGrip
- Generic name
- Extra-gynaecological surgical mesh, composite-polymer
- Model / reference
- ADG1510
- Primary DI / UDI-DI
- 10884521851672
- 510(k) Number
- FDA product code
- FTL
- GMDN term
- Extra-gynaecological surgical mesh, composite-polymer
- Device class
- Class II
- Regulation number
- 878.3300
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Size
- Width — 10 CentimeterLength — 15 Centimeter
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