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Ebner Medical LLC

United Statesfrom the FDA registration address FDA establishment FEI 1000222207

Ebner Medical LLC is a medical device manufacturer, with 1,061 devices listed in FDA GUDID (FDA Class I and II) as of 12 Nov 2026.

Devices
1,061
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 1,061
Device classes
  • FDA Class I 618
  • FDA Class II 443
Identifiers
  • FDA FEI 1000222207

What Ebner Medical LLC makes

EBNER MEDICAL LLC manufactures reusable surgical instruments including spinal rongeurs, craniofacial rongeurs, general-purpose surgical scissors, bone curettes, suturing needle holders, and instrument trays, as well as non-illuminating reusable surgical/emergency suction cannulas and open-surgery dissectors.

The company's devices are classified as Class I and Class II and are listed in the FDA UDI registry.

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

Catalogue1,061

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Company details

FDA FEI number
1000222207
Address
555 Blanding Blvd Ste B, Orange Park, FL, 32073

Frequently asked questions

How many devices does EBNER MEDICAL LLC have in the registry?

The registry currently lists 1061 devices for EBNER MEDICAL LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list EBNER MEDICAL LLC's devices?

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

What risk classes do EBNER MEDICAL LLC's devices fall under?

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

What are the newest devices from EBNER MEDICAL LLC in the registry?

The most recently registered devices listed for EBNER MEDICAL LLC include Ace Medical Company SW001-Box-5, Ace Medical CMVQT001-Box 10, Ace Medical Company SW001-Box-10 and Ace Medical CMVATD-S001 Box 100.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.