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Transilluminator, Ac-Powered
FDA product code HJM · Class 2 · Ophthalmic
34
Registered devices
7
Adverse events
3
Recalls
12
510(k) clearances
Devices with this code
FINOFF TRANSILLUMINATOR — Heine Optotechnik GmbH & Co. KGFINOFF TRANSILLUMINATOR — Heine Optotechnik GmbH & Co. KGFinhoff Transilluminator 2.8v — KEELER LIMITEDSynergetics — SYNERGETICS USA, INC.Acculite™ EndoOcular® — LUMENIS INC.OPHTHALMIC EXAMINATION LAMP — Heine Optotechnik GmbH & Co. KGESI — FTT MEDICAL, INC.ESI — FTT MEDICAL, INC.Synergetics — SYNERGETICS USA, INC.NeoGlo® Disposable — Neotech Products LLCTransilluminator 3.5v in carton — KEELER LIMITEDAcculite™ EndoOcular® — LUMENIS INC.NeoGlo® Disposable — Neotech Products LLCWALL TRANSFORMER EN 200-1 — Heine Optotechnik GmbH & Co. KG20GA Wide Angle Light Pipe - DORC — Peregrine Surgical, LlcVortex Surgical Inc. — Vortex Surgical, Inc.20GA Wide Angle Light Pipe - 297 Connector — Peregrine Surgical, LlcSynergetics — SYNERGETICS USA, INC.20GA Wide Angle Light Pipe - Standard — Peregrine Surgical, LlcSynergetics — SYNERGETICS USA, INC.27GA Midfield Endoillumination Probe — Peregrine Surgical, LlcSynergetics — SYNERGETICS USA, INC.ESI — FTT MEDICAL, INC.WALL TRANSFORMER EN 200 — Heine Optotechnik GmbH & Co. KG
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-12-16 | Vortex Surgical Inc. | XXX |
| 2007-11-09 | Chiu Technical Corp | Device was marketed without a 510(k). |
| 2003-11-10 | Bausch & Lomb Inc | The CX9625 Light Pipe connector may overheat; this condition could result in the plastic connector that plugs into the Millennium Microsurgical System to malfun |
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