Home › Device types › HLF
Device, Measuring, Lens Radius, Ophthalmic
FDA product code HLF · Class 1 · Ophthalmic
116
Registered devices
0
Adverse events
1
Recalls
3
510(k) clearances
Devices with this code
LASIK Cannulas — AURORA SURGICAL, LLCHoffer Optical Zone Marker — AURORA SURGICAL, LLCLasik Markers — AURORA SURGICAL, LLCLRI/Toric Markers — AURORA SURGICAL, LLCDSEK Markers — AURORA SURGICAL, LLCLasik Fixation Ring — AURORA SURGICAL, LLCToric IOL Axis Marker w/2.5mm Radial, For Use with Beveled Degree Gauge, Titaniu — AURORA SURGICAL, LLCBores Axis Marker — AURORA SURGICAL, LLCDSEK Markers — AURORA SURGICAL, LLCHoffer Optical Zone Marker — AURORA SURGICAL, LLCLasik Markers — AURORA SURGICAL, LLCHoffer Optical Zone Marker, With Cross Hairs, 4mm, Titanium — AURORA SURGICAL, LLCPRK, LASIK, LASEK, IntraLasik and Flap Management Instruments — AURORA SURGICAL, LLCHoffer Optical Zone Marker, With Cross Hairs, 4.5mm, Titanium — AURORA SURGICAL, LLCDSEK Markers — AURORA SURGICAL, LLCMedetz Surgical Instruments — Medetz Surgical Instruments LLCCentration Marker — AURORA SURGICAL, LLCLASIK Cannulas — AURORA SURGICAL, LLCCorneal Markers — AURORA SURGICAL, LLCMarker — AURORA SURGICAL, LLCPRK, LASIK, LASEK, IntraLasik and Flap Management Instruments — AURORA SURGICAL, LLCCorneal Markers — AURORA SURGICAL, LLCBLADE BREAKERS AND HOLDERS — AURORA SURGICAL, LLCLASIK Cannulas — AURORA SURGICAL, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-05-19 | Haag-Streit USA Inc | During the creation of the Lenstar LS 900 software, the ability to perform a manual adjustment of the retinal thickness measurement was not disabled for product |
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