Home › Device types › HNL
Probe, Lachrymal
FDA product code HNL · Class 1 · Ophthalmic
659
Registered devices
40
Adverse events
1
Recalls
10
510(k) clearances
Devices with this code
BOWMAN LACRIMAL PROBE — SONTEC INSTRUMENTS, INC.Aztec — Aztecmed/Ent LLCAztec — Aztecmed/Ent LLCIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONWalcott Rx Products — Walcott Rx Product IncN.A. — Geuder AktiengesellschaftRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHELMED INCORPORATED — ELMED INCORPORATEDSymmetry Tyrell — ASPEN SURGICAL PRODUCTS, INC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONAnodyne Surgical — Psi/Eye-Ko, Inc.V. Mueller — STERIS CORPORATIONPROBE — KLS-Martin L.P.BR Surgical, LLC — BR Surgical, LLCMSI Precision Specialty Instruments — Med Saver, Inc.Ambler Surgical — AMBLER SURGICAL CORP.N.A. — Geuder AktiengesellschaftMSI Precision Specialty Instruments — Med Saver, Inc.Ambler Surgical — AMBLER SURGICAL CORP.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHRumex — RUMEX INTERNATIONAL CORP.MR PHACO — Crestpoint Management LimitedBausch + Lomb — Bausch & Lomb IncorporatedMillennium — Avalign Technologies, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-26 | Quest Medical, Inc. | Expiration date incorrectly printed in Manufacturing Date field on both pouch and carton labels |
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