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Transilluminator, Battery-Powered

FDA product code HJN · Class 1 · Ophthalmic

46
Registered devices
24
Adverse events
1
Recalls
3
510(k) clearances

Devices with this code

NeoGlo® — Neotech Products LLCzumax — Zumax Medical Co., LTDFINOFF TRANSILLUMINATOR — Heine Optotechnik GmbH & Co. KGVenoscope — VENOSCOPE, LLCFINOFF TRANSILLUMINATOR — Heine Optotechnik GmbH & Co. KGWelch Allyn, Inc. — WELCH ALLYN, INC.LUMINDEX — DENTMATE TECHNOLOGY CO., LTD.Welch Allyn, Inc. — WELCH ALLYN, INC.OPHTHALMIC EXAMINATION LAMP — Heine Optotechnik GmbH & Co. KGNeoGlo® — Neotech Products LLCWelch Allyn, Inc. — WELCH ALLYN, INC.NeoGlo Disposable — Neotech Products LLCzumax — Zumax Medical Co., LTDWelch Allyn, Inc. — WELCH ALLYN, INC.Amico Diagnostic Illuminator — Amico Diagnostic IncorporatedEZ-TRI-3600 — U.S. OPHTHALMIC, L.L.C.ESU TRANSILLUMINATOR — ESU LIMITED LIABILITY PARTNERSHIPAmico Diagnostic Illuminator — Amico Diagnostic IncorporatedNeoGlo® — Neotech Products LLCNeoGlo Disposable — Neotech Products LLCWelch Allyn, Inc. — WELCH ALLYN, INC.Bernell — BernellNeoGlo® — Neotech Products LLCNeoGlo® — Neotech Products LLC

Recent recalls

DateFirmReason
2005-04-28Venoscope LLCExcessive heating due to incorrect wire assembly process.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.