Kontact K30PA754
Kontact K30PA754 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 03701045233114), 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 | Number03701045233114 | Date1 Dec 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK210220 | Date18 Jun 2021 | StatusActive |
Official records
- AccessGUDID record 03701045233114
- FDA 510(k) database K210220
Across registries
- FDA 510(k) K210220 decided 18 Jun 2021 Active
- FDA GUDID UDI-DI 03701045233114 listed 1 Dec 2021 Listed
Timeline
- Cleared FDA 510(k) K210220
- Listed FDA GUDID 03701045233114
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Kontact
- Generic name
- Dental implant system
- Model / reference
- K30PA754
- Primary DI / UDI-DI
- 03701045233114
- 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
Similar devices in this category
Other devices filed under Dental implant system.
- Neobiotech Implant System ITW316007AP by Neobiotech Co.,Ltd.
- Biotem HAA452S by Biotem Co., ltd
- Neobiotech Implant System ISAE455 by Neobiotech Co.,Ltd.
- Biotem SABT40535 by Biotem Co., ltd
- IU Fixture FIU45100 by WARANTEC.Co., Ltd
- RN Octagon angled Abutment 032160 by BIO CONCEPT Co., Ltd.
- Magic FC II FC6007 by InnoBioSurg Co., Ltd(IBS implant Co., Ltd)