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Ninomed LLC

Active in EUDAMED

Registered as NinoMed in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000037124 FEI 3011336784

Devices
5
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

What Ninomed LLC makes

Ninomed LLC manufactures reusable patient positioning pads designed to support and stabilize patients during medical procedures, including those in the STS-BodyPad™ series (Regular Plus, Regular, and XL Plus). These devices are intended for use in surgical and procedural settings to enhance patient comfort and reduce operator fatigue by providing adjustable support and cushioning.

The company’s products are classified as Class I medical devices and are registered in the EU’s eudamed database. Ninomed LLC is based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

Company details

EUDAMED SRN
US-MF-000037124
FDA FEI number
3011336784
EUDAMED status
Active
EUDAMED registered name
NinoMed
Registered address
241, Parker Road, 27517, Chapel Hill, United States
Phone
919-818-3711
PRRC contact
Anthony Visco(public in EUDAMED)

Frequently asked questions

How many devices does NINOMED LLC have in the registry?

The registry currently lists 5 devices for NINOMED LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list NINOMED LLC's devices?

Among its 5 most recently registered devices, NINOMED LLC has devices listed in EUDAMED (5 devices).

What risk classes do NINOMED LLC's devices fall under?

Among its 5 most recently registered devices, the classes recorded for NINOMED LLC's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from NINOMED LLC in the registry?

The most recently registered devices listed for NINOMED LLC include STS-BodyPad™- XL, Safe-T-Secure, STS-BodyPad™- Regular Plus and STS-BodyPad™- Regular.

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