# Moria SA > Medical device manufacturer record on deviCERTS, compiled from public registries. 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. - Canonical page: - Also registered as: Moria, Inc. - Country: France (FDA applicant, unverified) - Role: Manufacturer - DUNS: 275937506 ## Figures - Devices: 34 - FDA recalls (matched to the firm by name): 0 ## Registry facts *Every device of the manufacturer. A device listed in two registries counts in both.* - Registries: FDA GUDID 26, FDA 510(k) 8 - Device classes: FDA Class I 34 ## Devices The first 34 of 34, in the order of the canonical page, which lists them all. - [Moria Dual Action Sinskey Manipulator](https://devicerts.com/devices/moria-dual-action-sinskey-manipulator-20067) · Class I · GUDID · status: Listed - [Moria Dual Action Curved Scraper](https://devicerts.com/devices/moria-dual-action-curved-scraper-20068) · Class I · GUDID · status: Listed - [MORIA Vacuum Trephine - Adjustable 4.00 mm](https://devicerts.com/devices/moria-vacuum-trephine-adjustable-4-00-mm-17202d400) · Class I · GUDID · status: Listed - [Moria Epi-K Set (-1 Ring)](https://devicerts.com/devices/moria-epi-k-set-1-ring-19384) · Class I · GUDID · status: Listed - [Moria Epi-K Reusable Suction Ring 0](https://devicerts.com/devices/moria-epi-k-reusable-suction-ring-0-19389-0) · Class I · GUDID · status: Listed - [Moria Ou Lc 250 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-250) · Class I · GUDID · status: Withdrawn - [Moria Ou Lc 450 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-450) · Class I · GUDID · status: Listed - [Moria Cbsu 350 Head - Art. Chamber](https://devicerts.com/devices/moria-19178-350) · Class I · GUDID · status: Listed - [MORIA Bonn forceps](https://devicerts.com/devices/moria-20202x1) · Class I · GUDID · status: Listed - [Moria Cbsu 300 Head - Art. Chamber](https://devicerts.com/devices/moria-19178-300) · Class I · GUDID · status: Listed - [Moria Ou Lc 130 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-130) · Class I · GUDID · status: Listed - [MORIA Tying forceps straight](https://devicerts.com/devices/moria-202032x1) · Class I · GUDID · status: Listed - [Moria Ou Lc 150 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-150) · Class I · GUDID · status: Listed - [MORIA ONE - Punch D10.00mm x1](https://devicerts.com/devices/moria-17200d1000) · Class I · GUDID · status: Listed - [Moria Cbsu 130 Head - Art. Chamber](https://devicerts.com/devices/moria-19178-130) · Class I · GUDID · status: Listed - [MORIA Artificial chamber guide ring for ALTK](https://devicerts.com/devices/moria-19164) · Class I · GUDID · status: Listed - [Moria Ou Lc 110 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-110) · Class I · GUDID · status: Listed - [Moria Ou Lc 300 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-300) · Class I · GUDID · status: Listed - [Moria Ou Lc 400 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-400) · Class I · GUDID · status: Listed - [Moria Ou Lc 350 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-350) · Class I · GUDID · status: Listed - [Moria Ou Lc 500 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-500) · Class I · GUDID · status: Listed - [Moria Ou Lc 200 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-200) · Class I · GUDID · status: Listed - [Moria Cbsu 90 Head - Art. Chamber](https://devicerts.com/devices/moria-19178-90) · Class I · GUDID · status: Listed - [Moria Cbsu 50 Head - Art. Chamber](https://devicerts.com/devices/moria-19178-50) · Class I · GUDID · status: Listed - [Moria Cbsu 250 Head - Art. Chamber](https://devicerts.com/devices/moria-19178-250) · Class I · GUDID · status: Listed - [Moria Ou Lc 550 Head Artificial Chamber](https://devicerts.com/devices/moria-19184-550) · Class I · GUDID · status: Listed - [One Up Disposable Keratome Head](https://devicerts.com/devices/one-up-disposable-keratome-head-hno) · ref K981742 · Class I · 510(k) · status: Active · decision 1998-08-25 - [Carriazo Barraquer Ii Microkeratome](https://devicerts.com/devices/carriazo-barraquer-ii-microkeratome-hmy) · ref K002191 · Class I · 510(k) · status: Active · decision 2000-10-12 - [Carriazo Barraquer Single Use Microkeratome](https://devicerts.com/devices/carriazo-barraquer-single-use-microkeratome-hmy) · ref K003594 · Class I · 510(k) · status: Active · decision 2001-03-09 - [Oneuse- Plus Microkeratome](https://devicerts.com/devices/oneuse-plus-microkeratome-hmy) · ref K040297 · Class I · 510(k) · status: Active · decision 2004-03-31 - [M2 Single Use Microkertome](https://devicerts.com/devices/m2-single-use-microkertome-hmy) · ref K022560 · Class I · 510(k) · status: Active · decision 2002-09-27 - [M3 Microkeratome](https://devicerts.com/devices/m3-microkeratome-hno) · ref K032836 · Class I · 510(k) · status: Active · decision 2004-06-18 - [Carriazo Barraquer Microkeratome](https://devicerts.com/devices/carriazo-barraquer-microkeratome-hmy) · ref K981741 · Class I · 510(k) · status: Active · decision 1998-07-24 - [EPI K Console](https://devicerts.com/devices/epi-k-console-hno) · ref K172994 · Class I · 510(k) · status: Active · decision 2017-10-26 ## Source and citation - Cite as: Moria SA. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/moria-sa (data as of 2026-11-15). - Data sources: [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/) - FDA recall data as of: 2026-11-01 - Data as of: 2026-11-15 - JSON: - Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms. - Attribution: DevicErts, https://devicerts.com/manufacturers/moria-sa - Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.