Kontact K30P3
Kontact K30P3 is a Class II device made by Biotech Dental, cleared under FDA 510(k) K210220 on 18 Jun 2021 and listed in FDA GUDID since 1 Dec 2021 (UDI-DI 03701045233862), active as of 22 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 | Number03701045233862 | Date1 Dec 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK210220 | Date18 Jun 2021 | StatusActive |
Official records
- AccessGUDID record 03701045233862
- FDA 510(k) database K210220
Across registries
- FDA 510(k) K210220 decided 18 Jun 2021 Active
- FDA GUDID UDI-DI 03701045233862 listed 1 Dec 2021 Listed
Timeline
- Cleared FDA 510(k) K210220
- Listed FDA GUDID 03701045233862
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Kontact
- Generic name
- Dental implant system
- Model / reference
- K30P3
- Primary DI / UDI-DI
- 03701045233862
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Dental implant system
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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