AIR-FLOW b
by E.M.S. Electro Medical Systems S.A. 55 variants
AIR-FLOW b (EQ-160) is a Class I device made by E.M.S. Electro Medical Systems S.A., cleared under FDA 510(k) K110173 on 7 Apr 2011 and listed in FDA GUDID since 22 Sep 2016 (UDI-DI 07613353050900), 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 | Number07613353050900 | Date22 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK110173 | Date7 Apr 2011 | StatusActive |
Official records
- AccessGUDID record 07613353050900
- FDA 510(k) database K110173
Across registries
- FDA 510(k) K110173 decided 7 Apr 2011 Active
- FDA GUDID UDI-DI 07613353050900 listed 22 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K110173
- Listed FDA GUDID 07613353050900
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Air-Flow
- Generic name
- Chairside dental abrasive air jet system
- Model / Ref / Catalog
- b, EQ-160
- Primary DI / UDI-DI
- 07613353050900
- 510(k) Number
- FDA product code
- EFB
- GMDN term
- Chairside dental abrasive air jet system
- Device class
- Class I
- Regulation number
- 872.4200
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization