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Ahp Eos Buyer, Inc.

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Devices
4

What Ahp Eos Buyer, Inc. makes

Ahp Eos Buyer, Inc. makes medical devices such as bone growth stimulators, including the ORTHOPAK(R) BONE GROWTH STIMULATOR and the OSTEOSTIM(R), as well as spinal fusion stimulators like the SPF SPINAL FUSION STIMULATOR.

The company's portfolio is regulated as Class III devices and is listed in the FDA's Premarket Approval (PMA) registry, with the company based in the US.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Orthopak(R) Bone Growth Stimulator Ref P850022 Open recall

    Active Regimes: PMA Registry: PMA Class:—
  • Osteostim(R) Ref P790005

    Active Regimes: PMA Registry: PMA Class:III
  • Spf Spinal Fusion Stimulator Ref P850035

    Active Regimes: PMA Registry: PMA Class:III
  • Biomet Bhs- Mini Ref P790002

    Active Regimes: PMA Registry: PMA Class:—

Frequently asked questions

How many devices does Ahp Eos Buyer, Inc. have in the registry?

The registry currently lists 4 devices for Ahp Eos Buyer, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ahp Eos Buyer, Inc.'s devices?

Among its 4 most recently registered devices, Ahp Eos Buyer, Inc. has devices listed in FDA PMA (4 devices).

What risk classes do Ahp Eos Buyer, Inc.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Ahp Eos Buyer, Inc.'s devices are Class III. Each device page shows its own class and authorisation.

What are the newest devices from Ahp Eos Buyer, Inc. in the registry?

The most recently registered devices listed for Ahp Eos Buyer, Inc. include ORTHOPAK(R) BONE GROWTH STIMULATOR, OSTEOSTIM(R), SPF SPINAL FUSION STIMULATOR and BIOMET BHS- MINI.

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