# K082791: Ems Air-Flow Master

- Pathway: 510(k) (Traditional)
- Applicant: E.M.S Electro Medical Systems S.A
- Decided: Feb 18, 2009 after 148 days
- Product code: EFB (Handpiece, Air-Powered, Dental)
- Device class: 1
- Regulation: 21 CFR 872.4200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K900709 (1990). 2 ancestors in all.
23 later devices descend from it; 6 cite it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073284: Air-Flow Master Standard, (Ems Sa) Electro Medical Systems (2007) Summary page 1.

## Most influential descendants
- K092289: Ems Air-Flow Handy Perio (2009), 18 descendants of its own
- K110173: Ems Air-Flow Master Piezon (2011), 13 descendants of its own
- K190124: EMS AIRFLOW Prophylaxis Master, EMS AIRFLOW One (2019), 4 descendants of its own
- K132480: Air-Flow Handy 3.0 Perio (2014), 4 descendants of its own
- K132478: Air-Flow Handy 3.0 (2014), 3 descendants of its own

## Indications for use
The EMS AIR-FLOW MASTER is intended for patients suffering from periodontal disease and peri-implantitis. The EMS AIR-FLOW MASTER is indicated for the-non-surgical removal of subgingival plaque in pockets up to 5 mm after initial periodontal treatment.

Source page: https://510kreport.com/device/K082791
Methodology: https://510kreport.com/methodology