WSK10
Part of a family of 75 devices: see the family page
Ref WSK10
WSK10 is a Class I device made by ZimVie US Corp LLC, registered in EUDAMED on 3 Jun 2026 (Basic UDI-DI 844868A5H2) and listed in FDA GUDID since 31 Mar 2016 (UDI-DI 00844868018087), active as of 24 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number844868A5H2 00844868018087 | Date3 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00844868018087 | Date31 Mar 2016 | StatusListed |
Official records
- EUDAMED public site 844868A5H2
- AccessGUDID record 00844868018087
Across registries
- EUDAMED Basic UDI-DI 844868A5H2 registered 3 Jun 2026 Active
- FDA GUDID UDI-DI 00844868018087 listed 31 Mar 2016 Listed
Timeline
- Listed FDA GUDID 00844868018087
- Registered EUDAMED 844868A5H2
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Dental prosthesis/implant abutment screw analog, reusable
- Device name
- Dental Laboratory Tools
- Model / reference
- WSK10
- Primary DI / UDI-DI
- 00844868018087
- Basic UDI-DI
- 844868A5H2
- FDA product code
- NDP
- EMDN code
- Q0199 Odontology devices - other
- GMDN term
- Dental prosthesis/implant abutment screw analog, reusable
- Device class
- Class I
- Regulation number
- 872.3980
- EU registration type
- Standard device
- EU market of registration
- Spain
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 10 Millimeter
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