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
N.A. — Geuder AktiengesellschaftSCHEPENS SCLERAL DEPRESSOR — SONTEC INSTRUMENTS, INC.Novo Surgical Inc. — NOVO SURGICAL, INC.Scleral Depressors — AURORA SURGICAL, LLCScleral Depressor — SONTEC INSTRUMENTS, INC.SCHEPENS SCLERAL DEPRESSOR SMALL — KATENA PRODUCTS, INC.Millennium — Avalign Technologies, Inc.AESCULAP — AESCULAP, INC.V. Mueller — STERIS CORPORATIONBausch + Lomb — Bausch & Lomb IncorporatedOrbit Depressor — KATENA PRODUCTS, INC.HNM MEDICAL — HNM STAINLESS, LLC.Ambler Surgical — AMBLER SURGICAL CORP.HNM MEDICAL — HNM STAINLESS, LLC.PACKO SCLERAL DEPRESSOR WITH MARKER — KATENA PRODUCTS, INC.Scleral Depressors — AURORA SURGICAL, LLCHayden Medical — Hayden Medical, Inc.Stephens Instruments — KRISHNA IMPORTS INCScleral Depressors — AURORA SURGICAL, LLCONE — MORIA SAMR PHACO — Crestpoint Management LimitedPILLING — TELEFLEX INCORPORATEDScleral Depressors — AURORA SURGICAL, LLCV. Mueller — STERIS CORPORATION
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.
