Home › Device types › HNX
Depressor, Orbital
FDA product code HNX · Class 1 · Ophthalmic
149
Registered devices
11
Adverse events
0
Recalls
2
510(k) clearances
Devices with this code
Bausch + Lomb — Bausch & Lomb IncorporatedScleral Depressors — AURORA SURGICAL, LLCMSI Precision Specialty Instruments — Med Saver, Inc.MR PHACO — Crestpoint Management LimitedNA — DEPUY MITEK, LLCMSI Precision Specialty Instruments — Med Saver, Inc.Rumex — RUMEX INTERNATIONAL CORP.V. Mueller — STERIS CORPORATIONOrbit Depressor — KATENA PRODUCTS, INC.HNM MEDICAL — HNM STAINLESS, LLC.INAMI — INAMI & CO., LTD.PILLING — TELEFLEX INCORPORATEDScleral Depressors — AURORA SURGICAL, LLCScleral Depressors — AURORA SURGICAL, LLCSCHEPENS SCLERAL DEPRESSOR LARGE — KATENA PRODUCTS, INC.ONE — MORIA SAV. Mueller — STERIS CORPORATIONPILLING — TELEFLEX INCORPORATEDStephens Instruments — KRISHNA IMPORTS INCSymmetry Flynn — ASPEN SURGICAL PRODUCTS, INC.NA — DEPUY MITEK, LLCHNM MEDICAL — HNM STAINLESS, LLC.Scleral Depressors — AURORA SURGICAL, LLCOrbit Depressor — KATENA PRODUCTS, 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.
