Syneture VLOCN0317
by Covidien LP
Syneture VLOCN0317 is a Class II device made by Covidien LP, cleared under FDA 510(k) K103052 on 10 Nov 2010 and listed in FDA GUDID since 12 Jun 2019 (UDI-DI 10884521780231), 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 | Number10884521780231 | Date12 Jun 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK103052 | Date10 Nov 2010 | StatusActive |
Official records
- AccessGUDID record 10884521780231
- FDA 510(k) database K103052
Across registries
- FDA 510(k) K103052 decided 10 Nov 2010 Active
- FDA GUDID UDI-DI 10884521780231 listed 12 Jun 2019 Listed
Timeline
- Cleared FDA 510(k) K103052
- Listed FDA GUDID 10884521780231
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Syneture
- Generic name
- Barbed polyester suture, non-antimicrobial
- Model / reference
- VLOCN0317
- Primary DI / UDI-DI
- 10884521780231
- 510(k) Number
- FDA product code
- GAT
- GMDN term
- Barbed polyester suture, non-antimicrobial
- Device class
- Class II
- Regulation number
- 878.5000
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 12 Inch
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