Ophthalmoscope, Laser, Scanning
Ophthalmic · 21 CFR 886.1570
Recent MDR events
4 adverse event reports on file
Event type breakdown
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
40 firms currently registered for this product code
Wild Gmbh
Voelkermarkt Karnten, AT
Centervue
Padova Veneto, IT
Optos Plc
DUNFERMLINE, FIFE, GB
Kowa Co. Ltd. Chofu
Chofu Tokyo, JP
Mw.fep Spa
San Giovanni in Persiceto Bologna, IT
Elemaster Spa
lomagna Lecco, IT
Nidek Co., Ltd. Hamacho Plant
GAMAGORI, AICHI, JP
Nidek Incorporated
The Colony, TX, US
Optos Inc.
Southborough, MA, US
Carl Zeiss Meditec Inc
DUBLIN, CA, US
Fedex Supply Chain, Inc.
Memphis, TN, US
Ocusciences, Inc.
Ann Arbor, MI, US
Nidek Co., Ltd.
GAMAGORI, AICHI, JP
Heidelberg Engineering Gmbh
HEIDELBERG Baden-Wurttemberg, DE
510(k) clearances
22 clearances for this product code
- Ocusciences, Inc.Apr 22, 2025
K241931 · OcuMet Beacon (OCUB100)
- Centervue S.P.A.Mar 17, 2025
K243504 · MAIA (AHMACME001)
- Centervue S.P.A.Dec 21, 2021
K213705 · DRSplus
- Centervue S.P.A.Aug 19, 2021
K211328 · EIDON FA, EIDON, EIDON AF, EIDON UWFL
- Centervue S.P.A.Nov 15, 2019
K192113 · DRSplus
- Centervue S.P.A.Jul 16, 2018
K180526 · EIDON FA
- Centervue S.P.A.May 30, 2018
K180293 · Retia 2
- Centervue S.P.A.Jun 8, 2016
K153181 · MAIA