Moria SA
FranceFDA applicant, unverified
Moria SA is a medical device manufacturer, with 34 devices listed in FDA GUDID and FDA 510(k) (FDA Class I) as of 15 Nov 2026.
- Devices
- 34
Registry facts
- Registries
- FDA GUDID 26
- FDA 510(k) 8
- Device classes
- FDA Class I 34
- Identifiers
- DUNS 275937506
What Moria SA makes
Moria SA manufactures reusable ophthalmic surgical instruments, including microkeratomes for corneal cutting, soft-tissue manipulation forceps, corneal punch sets, and corneal resection holders. These tools are designed for precision procedures in refractive and corneal surgeries, such as LASIK and lamellar keratoplasty.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via 510(k) premarket notifications and the FDA’s Unique Device Identifier (UDI) system.
Catalogue
Search and filter all 34 devicesCompany details
- DUNS number
- 275937506
Frequently asked questions
How many devices does Moria SA have in the registry?
The registry currently lists 34 devices for Moria SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Moria SA's devices?
Among its 34 most recently registered devices, Moria SA has devices listed in FDA 510(k) (8 devices) and FDA GUDID (26 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Moria SA's devices fall under?
Among its 34 most recently registered devices, the classes recorded for Moria SA's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Moria SA in the registry?
The most recently registered devices listed for Moria SA include MORIA DUAL ACTION SINSKEY MANIPULATOR, MORIA DUAL ACTION CURVED SCRAPER, MORIA Vacuum Trephine - Adjustable 4.00 mm and MORIA EPI-K SET (-1 RING).