Quill VLP-4160
by Surgical Specialties México, S. de R.L. de C.V.
Quill VLP-4160 is a Class II device made by Surgical Specialties México, S. de R.L. de C.V., cleared under FDA 510(k) K132268 on 23 Aug 2013 and listed in FDA GUDID since 11 Jul 2025 (UDI-DI 00848782051519), 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 | Number00848782051519 | Date11 Jul 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK132268 | Date23 Aug 2013 | StatusActive |
Official records
- AccessGUDID record 00848782051519
- FDA 510(k) database K132268
Across registries
- FDA 510(k) K132268 decided 23 Aug 2013 Active
- FDA GUDID UDI-DI 00848782051519 listed 11 Jul 2025 Listed
Timeline
- Cleared FDA 510(k) K132268
- Listed FDA GUDID 00848782051519
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Quill
- Generic name
- Barbed polyester suture, non-antimicrobial
- Model / reference
- VLP-4160
- Primary DI / UDI-DI
- 00848782051519
- 510(k) Number
- FDA product code
- NEW
- GMDN term
- Barbed polyester suture, non-antimicrobial
- Device class
- Class II
- Regulation number
- 878.4840
- GUDID distribution status
- In Commercial Distribution
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