Trexon SY5690P
by Covidien LP
Trexon SY5690P is a Class II device made by Covidien LP, cleared under FDA 510(k) K253530 on 28 May 2026 and listed in FDA GUDID since 10 Oct 2026 (UDI-DI 10884521840683), 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 | Number10884521840683 | Date10 Oct 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK253530 | Date28 May 2026 | StatusActive |
Official records
- AccessGUDID record 10884521840683
- FDA 510(k) database K253530
Across registries
- FDA 510(k) K253530 decided 28 May 2026 Active
- FDA GUDID UDI-DI 10884521840683 listed 10 Oct 2026 Listed
Timeline
- Cleared FDA 510(k) K253530
- Listed FDA GUDID 10884521840683
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Trexon
- Generic name
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial
- Model / reference
- SY5690P
- Primary DI / UDI-DI
- 10884521840683
- 510(k) Number
- FDA product code
- GAM
- GMDN term
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial
- Device class
- Class II
- Regulation number
- 878.4493
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Size
- Length — 18 Inch