Home › Device types › EQH
Source, Carrier, Fiberoptic Light
FDA product code EQH · Class 1 · Ear, Nose, Throat
700
Registered devices
36
Adverse events
1
Recalls
49
510(k) clearances
Devices with this code
PILLING — TELEFLEX INCORPORATEDMSI Precision Specialty Instruments — Med Saver, Inc.NA — SCHÖLLY FIBEROPTIC GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHPILLING — TELEFLEX INCORPORATEDPILLING — TELEFLEX INCORPORATEDPILLING — TELEFLEX INCORPORATEDRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHELMED INCORPORATED — ELMED INCORPORATEDPILLING — TELEFLEX INCORPORATEDMillennium — Avalign Technologies, Inc.mytaMed — Mytamed, Inc.PILLING — TELEFLEX INCORPORATEDNovo Surgical Inc. — NOVO SURGICAL, INC.Ambler Surgical — AMBLER SURGICAL CORP.Millennium — Avalign Technologies, Inc.PILLING — TELEFLEX INCORPORATEDMillennium — Avalign Technologies, Inc.MicroFrance® — INTEGRA MICROFRANCEELMED — ELMED INCORPORATEDPILLING — TELEFLEX INCORPORATEDELMED — ELMED INCORPORATEDFiberglass light carrier — Spiggle & Theis Medizintechnik GmbHMarina Medical — MARINA MEDICAL INSTRUMENTS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-02-07 | Boston Scientific Corporation | Light Degradation in transmission-A film may deposit on the front face and limit transmission of light |
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