Customed 712057712782
Customed 712057712782 (9002782) is a Class II device made by Customed, Inc., cleared under FDA 510(k) K050887 on 11 Jul 2005 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI M20890027823), 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 | NumberM20890027823 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK050887 | Date11 Jul 2005 | StatusActive |
Official records
- FDA 510(k) database K050887
Across registries
- FDA 510(k) K050887 decided 11 Jul 2005 Active
- FDA GUDID UDI-DI M20890027823 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K050887
- Listed FDA GUDID M20890027823
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Customed
- Generic name
- Vaginal speculum, single-use
- Model / Ref / Catalog
- 712057712782, 9002782
- Primary DI / UDI-DI
- M20890027823
- 510(k) Number
- FDA product code
- HIB
- GMDN term
- Vaginal speculum, single-use
- Device class
- Class II
- Regulation number
- 884.4530
- GUDID distribution status
- In Commercial Distribution
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