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Easter Services, Inc.

United StatesFDA applicant, unverified

Devices
2

What Easter Services, Inc. makes

Easter Services, Inc. manufactures the EASTERCLAVE, a medical device designed for orthopedic fixation, likely used in bone stabilization procedures.

The EASTERCLAVE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Easterclave Ref K951557

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Easterclave Ref K961230

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Easter Services, Inc. have in the registry?

The registry currently lists 2 devices for Easter Services, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Easter Services, Inc.'s devices?

Among its 2 most recently registered devices, Easter Services, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Easter Services, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Easter Services, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Easter Services, Inc. in the registry?

The most recently registered devices listed for Easter Services, Inc. include EASTERCLAVE.

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