Skip to content

Rmo

Active in EUDAMED
Also registered as Rmo, Inc.

United Statesfrom SRN EUDAMED FDA SRN US-MF-000034842 FEI 1718476

Devices
3,884
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI
Authorised rep.
Rmo EuropeFR

What Rmo makes

RMO manufactures orthodontic devices including metal and ceramic brackets, archwires, tubes, metal bands, wires, pliers, and single-use plastic brackets.

The company's products are listed in the FDA UDI registry and include Class I and Class II devices. RMO is based in the US.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3,884

Newest first, rows 1-50 of 3,884

Search and filter all 3,884 devices
Skip device list

Rows 1-50 of 3,884

Showing 1-50 of 3,884

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000034842
FDA FEI number
1718476
EUDAMED status
Active
EUDAMED registered name
RMO
Registered address
2165, Earlywood Dr, 46131, Franklin, United States
PRRC contact
Grace McColley(public in EUDAMED)

Frequently asked questions

How many devices does RMO have in the registry?

The registry currently lists 3884 devices for RMO. Devices recorded under merged duplicate company entries are counted once.

Which registries list RMO's devices?

Among its 50 most recently registered devices, RMO has devices listed in FDA GUDID (50 devices).

What risk classes do RMO's devices fall under?

Among its 50 most recently registered devices, the classes recorded for RMO's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from RMO in the registry?

The most recently registered devices listed for RMO include FLI Q07536, RMO A06110, Mini-Taurus M01159 and FLI Orthonol A07013-A.

Generated automatically from registry data and not verified by a human reviewer.