Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3000264417

FEI Number

3000264417

Entity Name

Moria S.A

City/State/Country

Bourbon l'Archambault Allier, FR

Establishment Address

27 rue du pied de fourche, Bourbon l'Archambault Allier 03160, FR

Establishment Type(s)

Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Moria S.A. (Owner Number: 9029102)

Owner / Operator Contact Address

23 Avenue Carnot, 3 Rue Christophe Colomb, MASSY, FR-92 91300, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Microsurgical, instruments tray ST-T1 Microsurgical, instruments tray ST-L1 Microsurgical, instruments tray ST-S1 20047_HOFFART HOOK 20046_TANITO HOOK 205_SILASTIC METER REF. 205

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GZX	Instrument, Microsurgical	Neurology	Class 1	882.4525	1997-01-10
JYQ	Loop, Wire	Ear, Nose, Throat	Class 1	874.4420	1997-01-10
HMY	Keratome, Battery-Powered	Ophthalmic	Class 1	886.4370	2008-01-17
HNR	Forceps, Ophthalmic	Ophthalmic	Class 1	886.4350	1997-01-10
HMY	Keratome, Battery-Powered	Ophthalmic	Class 1	886.4370	2008-11-12
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2019-03-26
HNF	Scissors, Ophthalmic	Ophthalmic	Class 1	886.4350	1997-01-10
HND	Spatula, Ophthalmic	Ophthalmic	Class 1	886.4350	1997-01-10
HOE	Caliper, Ophthalmic	Ophthalmic	Class 1	886.4350	1997-01-10
HMY	Keratome, Battery-Powered	Ophthalmic	Class 1	886.4370	2008-11-12
HNL	Probe, Lachrymal	Ophthalmic	Class 1	886.4350	1997-01-10
HNH	Ring, Ophthalmic (Flieringa)	Ophthalmic	Class 1	886.4350	1997-01-10
HNQ	Hook, Ophthalmic	Ophthalmic	Class 1	886.4350	1997-01-10
GEY	Motor, Surgical Instrument, Ac-Powered	General, Plastic Surgery	Class 1	878.4820	2017-12-06
HNO	Keratome, Ac-Powered	Ophthalmic	Class 1	886.4370	2008-11-12
HNZ	Curette, Ophthalmic	Ophthalmic	Class 1	886.4350	1997-01-10
HRH	Trephine, Manual, Ophthalmic	Ophthalmic	Class 1	886.4350	1997-01-10
HNO	Keratome, Ac-Powered	Ophthalmic	Class 1	886.4370	2008-11-12
GDZ	Handle, Scalpel	General, Plastic Surgery	Class 1	878.4800	1997-01-10
HNX	Depressor, Orbital	Ophthalmic	Class 1	886.4350	2007-10-18
HNN	Knife, Ophthalmic	Ophthalmic	Class 1	886.4350	1997-01-10
HNO	Keratome, Ac-Powered	Ophthalmic	Class 1	886.4370	2008-01-17
HNM	Needle, Ophthalmic Suturing	Ophthalmic	Class 1	886.4350	2019-03-07

Official Correspondent

Bruno Chermette

US Agent Details

James Kusters Business: Moria, Inc. Email: jkusters@moriausa.com Phone: (215) 2307662

Related Public Records

Same Entity

Moria S.A.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3016214537	Metal Process	Montevrain Ile-de-France, FR
9615659	MORIA S.A.	MASSY Hauts-de-Seine, FR
3011659857	Ophsurin Co., Ltd	Suqian Jiangsu, CN

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K905383	Micro Surgical Instruments Corp.	2710-000 OSCILLATING SAW, GENERAL ASSEMBLY	1991-06-18
K913369	Micro Surgical Instruments Corp.	MICRO-AIRE MODEL 2060	1991-11-01
K874057	Myocure, Inc.	OPHTHALMIC TIP & BLADE SCALPELS	1987-12-23

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0039-2018	Teleflex Medical	1	Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.
Z-0026-04	Surgical Specialties Corp	1	Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled. The product can be sold as an individual unit or in a box of 6 knives.
Z-1922-2024	Alcon Research LLC Aspex Facility	1	20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Z-1923-2024	Alcon Research LLC Aspex Facility	1	ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1924-2024	Alcon Research LLC Aspex Facility	1	ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3000264417. Last updated year: 2026. Please use registration number 3000264417 when referencing this establishment in official correspondence.