Home › Device types › HJO
Biomicroscope, Slit-Lamp, Ac-Powered
FDA product code HJO · Class 2 · Ophthalmic
413
Registered devices
217
Adverse events
8
Recalls
109
510(k) clearances
Devices with this code
PolyLock Small Bone — FUSION ORTHOPEDICS, LLCSLZ 5XP TBL USA — KEELER LIMITEDSLH 5XC LED DiR TBL — KEELER LIMITEDLUMENIS — COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRLSLZ 5XC Di TBL — KEELER LIMITEDVISIONIX — LUNEAU TECHNOLOGY OPERATIONSSLZ 5XC TBL USA — KEELER LIMITEDMARCO — TAKAGI SEIKO CO.,LTD.INAMI — INAMI & CO., LTD.PolyLock Ankle — FUSION ORTHOPEDICS, LLCESSILOR SL350L — ESSILOR INTERNATIONALLED SLIT LAMP — RIGHT MFG. CO., LTD.LuxVision — U.S. OPHTHALMIC, L.L.C.Zoom Slit Lamp — RIGHT MFG. CO., LTD.S4 OPTIK — COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRLMediWorks — SHANGHAI MEDIWORKS PRECISION INSTRUMENTS CO.,LTD.SLZ 5XP DiR TBL — KEELER LIMITEDOPTICAL BIOMETER — NIDEK CO.,LTD.ALADDIN-M — VISIA IMAGING SRLSLZ 5XP DiR REF — KEELER LIMITEDVISIONIX — LUNEAU TECHNOLOGY OPERATIONSALADDIN TMS — VISIA IMAGING SRLSLH 5XC 12V Di REF — KEELER LIMITEDTAKAGI — TAKAGI SEIKO CO.,LTD.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-04-15 | Haag-Streit USA Inc | Examination data and patient name may be mixed up when printing or generating a pdf with the interface at Pacific Coast and Laser Institute (PCLI). |
| 2020-12-07 | Carl Zeiss Meditec AG | When using software 1.90.2.09 or 1.90.8.06 and using modality worklist functionality for patient data transfer, the selection of the patient in the patient list |
| 2018-06-25 | Carl Zeiss Meditec AG | Calibration setting was incorrectly entered during manufacturing causing the optical coherence tomography (OCT) to obtain the incorrect two-dimensional images o |
| 2016-07-01 | Nidek Inc | Nidek Inc. received information from our manufacturer NIDEK CO. Japan that the shown axial lengths were much shorter at AL-Scan measurement. |
| 2015-10-27 | Carl Zeiss Meditec AG | IOL Master software versions 7.5 and 7.7 calculation printouts and exported reports can contain the wrong IOL power data. |
| 2015-10-27 | Carl Zeiss Meditec AG | IOL Master software versions 7.5 and 7.7 calculation printouts and exported reports can contain the wrong IOL power data. |
| 2013-10-23 | Carl Zeiss Meditec, Inc. | The user database delivered for download contained an erroneous value. Specifically the "aO" constant of the lens AMO Sensar AR40E is listed as "0.0" in the int |
| 2013-10-23 | Carl Zeiss Meditec, Inc. | The user database delivered for download contained an erroneous value. Specifically the "aO" constant of the lens AMO Sensar AR40E is listed as "0.0" in the int |
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.