DemeCAPRONE MO1070036B16P
DemeCAPRONE MO1070036B16P is a Class II device made by DemeTECH Corp, cleared under FDA 510(k) K130083 on 17 Jul 2013 and listed in FDA GUDID since 9 Jul 2019 (UDI-DI 10652927284864), 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 | Number10652927284864 | Date9 Jul 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK130083 | Date17 Jul 2013 | StatusActive |
Official records
- AccessGUDID record 10652927284864
- FDA 510(k) database K130083
Across registries
- FDA 510(k) K130083 decided 17 Jul 2013 Active
- FDA GUDID UDI-DI 10652927284864 listed 9 Jul 2019 Listed
Timeline
- Cleared FDA 510(k) K130083
- Listed FDA GUDID 10652927284864
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- DemeCAPRONE
- Generic name
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial
- Model / reference
- MO1070036B16P
- Primary DI / UDI-DI
- 10652927284864
- 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
Similar devices in this category
Other devices filed under Polyester suture, bioabsorbable, monofilament, non-antimicrobial.