Home › Device types › KAG
Holder, Speculum, Ent
FDA product code KAG · Class 1 · General, Plastic Surgery
22
Registered devices
1
Adverse events
0
Recalls
2
510(k) clearances
Devices with this code
AESCULAP — Aesculap AGLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHACE — ACE SURGICAL SUPPLY CO., INC.LAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHACE — ACE SURGICAL SUPPLY CO., INC.LAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHACE — ACE SURGICAL SUPPLY CO., INC.LAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbH
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
