Medical Device Manufacturer · FR , Cournon D'Auvergne-Cedex

Quantel Medical - FDA 510(k) Cleared Devices

30 submissions · 30 cleared · Since 2000

Recent clearances: INTEGRE LIO, Pocket III, Capsulo

Official Website

Total

Cleared

Denied

Quantel Medical has 30 FDA 510(k) cleared medical devices. Based in Cournon D'Auvergne-Cedex, FR.

Latest FDA clearance: Feb 2026. Active since 2000. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Quantel Medical Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by O'Connell Regulatory Consultants, Inc. and Regulatory Technology Services, LLC.

Quantel Medical is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Quantel Medical

30 devices

1-12 of 30

Axialis Ophthalmic Ultrasound System

COMPACT TOUCH Ophthalmic Ultrasound System

OPTIMUS FUSION: SLT, YAG AND YAG/SLT

General & Plastic Surgery · 181d

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026

Quantel Medical - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Quantel Medical

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