Acteon Kit Perfect'margin Rounded
by Satelec
Acteon Kit Perfect'margin Rounded (F00738) is a Class II device made by Satelec, cleared under FDA 510(k) K132322 on 11 Mar 2014 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 03609820007380), 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 | Number03609820007380 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK132322 | Date11 Mar 2014 | StatusActive |
Official records
- AccessGUDID record 03609820007380
- FDA 510(k) database K132322
Across registries
- FDA 510(k) K132322 decided 11 Mar 2014 Active
- FDA GUDID UDI-DI 03609820007380 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K132322
- Listed FDA GUDID 03609820007380
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Acteon
- Generic name
- Ultrasonic dental scaling/debridement system handpiece tip, periodontal
- Model / Ref / Catalog
- KIT PERFECT'MARGIN ROUNDED, F00738
- Description
- PERFECTMARGIN® ROUNDED: quarter round shape tips, whose form is in harmony with burs used in supra-gingival.
- Primary DI / UDI-DI
- 03609820007380
- 510(k) Number
- FDA product code
- ELC
- GMDN term
- Ultrasonic dental scaling/debridement system handpiece tip, periodontal
- Device class
- Class II
- Regulation number
- 872.4850
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization