Skip to content

Allo Pro Corp.

United StatesFDA applicant, unverified

Devices
16

What Allo Pro Corp. makes

Allo Pro Corp. manufactures orthopedic implants for hip and elbow joints, including cementless hip endoprostheses, ceramic femoral heads, centering plugs, and modular hip components such as stems and acetabular cups. Their portfolio also includes polyethylene medullary plugs, femoral head prostheses, and elbow replacements like the GSB elbow system.

The company’s devices are classified under FDA categories Class I, Class II, and Class III, with submissions recorded in the FDA’s 510(k) registry. Products are listed under US regulatory requirements, reflecting their compliance with medical device authorisation pathways in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue16

Newest first, rows 1-16 of 16

Search and filter all 16 devices
Skip device list

  • Cementless Zweymueller Hip Endoprothes Ref K822979

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

  • Biolox Ceramic Ball Ref K892644

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

  • Centering Plug Ref K900392

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

  • Zweymuller Cup Ref K851213

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

  • Zweymueller-Sl Hip Prosthesis Stem Ref K871453

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

  • Gsb Elbow Ref K901581

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

  • Weber Permalock Ref K896669

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

  • Weber/Stiihmer Femoral Head Prosthesis Ref K830948

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

  • Kennedy Stem Ref K864999

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

  • Polyethylene Medullary Plug - Stiihmer/ Ref K830949

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

  • Weber/Stuehmer Hip Joint Endoprosthesis Ref K811119

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

  • Weber-Stuhmer Hip Prosthesis Stem Ref K841391

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

  • Rs-Cup Acetabular Prosthesis Ref K885049

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

  • Semi-Constraint Kee Joint Hinge Prosth Ref K811105

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

  • The Original Leinbach Platform Total Hip Ref K820755

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

  • Surgical Cotton Gloves Ref K900425

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

Rows 1-16 of 16

Frequently asked questions

How many devices does Allo Pro Corp. have in the registry?

The registry currently lists 16 devices for Allo Pro Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Allo Pro Corp.'s devices?

Among its 16 most recently registered devices, Allo Pro Corp. has devices listed in FDA 510(k) (16 devices).

What risk classes do Allo Pro Corp.'s devices fall under?

Among its 16 most recently registered devices, the classes recorded for Allo Pro Corp.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Allo Pro Corp. in the registry?

The most recently registered devices listed for Allo Pro Corp. include CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES, BIOLOX CERAMIC BALL, CENTERING PLUG and ZWEYMULLER CUP.

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