Home › Device types › EIX
Probe, Periodontic
FDA product code EIX · Class 1 · Dental
1,709
Registered devices
11
Adverse events
0
Recalls
9
510(k) clearances
Devices with this code
Nordent Manufacturing, Inc. — NORDENT MANUFACTURING INCAmerican Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.Surgical Direct — Surgical Direct, Inc.American Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.HU-FRIEDY — HU-FRIEDY MFG. CO., LLCAmerican Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.HU-FRIEDY — HU-FRIEDY MFG. CO., LLCPomee — POMEE CORPORATIONAmerican Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.Pomee — POMEE CORPORATIONHU-FRIEDY — HU-FRIEDY MFG. CO., LLCSurgical Direct — Surgical Direct, Inc.Surgical Direct — Surgical Direct, Inc.HU-FRIEDY — HU-FRIEDY MFG. CO., LLCHU-FRIEDY — HU-FRIEDY MFG. CO., LLCPower Dental U.S.A., Inc. — Power Dental U.S.A. Inc.American Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.Power Dental U.S.A., Inc. — Power Dental U.S.A. Inc.BAYLOR TACTILE TONE PERIDONTAL PROBE — SONTEC INSTRUMENTS, INC.Surgical Direct — Surgical Direct, Inc.Power Dental USA — Power Dental U.S.A. Inc.HU-FRIEDY — HU-FRIEDY MFG. CO., LLCAESCULAP — Aesculap AGPDT, Inc. — PDT, INC.
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.
