Sutumed SDAG001MR260
by Unilene Sac
Sutumed SDAG001MR260 is a Class II device made by Unilene Sac, cleared under FDA 510(k) K100780 on 14 Dec 2010 and listed in FDA GUDID since 7 Jan 2023 (UDI-DI 07757093000747), 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 | Number07757093000747 | Date7 Jan 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK100780 | Date14 Dec 2010 | StatusActive |
Official records
- AccessGUDID record 07757093000747
- FDA 510(k) database K100780
Across registries
- FDA 510(k) K100780 decided 14 Dec 2010 Active
- FDA GUDID UDI-DI 07757093000747 listed 7 Jan 2023 Listed
Timeline
- Cleared FDA 510(k) K100780
- Listed FDA GUDID 07757093000747
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Sutumed
- Generic name
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial
- Model / reference
- SDAG001MR260
- Primary DI / UDI-DI
- 07757093000747
- 510(k) Number
- FDA product code
- GAN
- GMDN term
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial
- Device class
- Class II
- Regulation number
- 878.4830
- GUDID distribution status
- In Commercial Distribution
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