Home › Device types › HJN
Transilluminator, Battery-Powered
FDA product code HJN · Class 1 · Ophthalmic
39
Registered devices
24
Adverse events
1
Recalls
3
510(k) clearances
Devices with this code
Welch Allyn, Inc. — WELCH ALLYN, INC.Welch Allyn, Inc. — WELCH ALLYN, INC.LUMINDEX — DENTMATE TECHNOLOGY CO., LTD.Venoscope — VENOSCOPE, LLCEZ-TRI-3600 — U.S. OPHTHALMIC, L.L.C.Welch Allyn, Inc. — WELCH ALLYN, INC.NeoGlo® — Neotech Products LLCAmico Diagnostic Illuminator — Amico Diagnostic IncorporatedLumindex 3 LED Transilluminator — PRACTICON, INC.VF1000LED Vein locator — FABINJECT INDUSTRIA E COMERCIO IMPORTACAO E EXPORTACAO LTDAAmico Diagnostic Illuminator — Amico Diagnostic IncorporatedNeoGlo® — Neotech Products LLCNeoGlo® — Neotech Products LLCASTODIA — Stihler Electronic GmbHLUMINDEX — DENTMATE TECHNOLOGY CO., LTD.NeoGlo® — Neotech Products LLCWelch Allyn, Inc. — WELCH ALLYN, INC.NeoGlo® — Neotech Products LLCNeoGlo® — Neotech Products LLCNeoGlo Disposable — Neotech Products LLCNeoGlo® — Neotech Products LLCOPHTHALMIC EXAMINATION LAMP — Heine Optotechnik GmbH & Co. KGVenoscope — VENOSCOPE, LLCWelch Allyn, Inc. — WELCH ALLYN, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-28 | Venoscope LLC | Excessive heating due to incorrect wire assembly process. |
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.