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Ace Orthopedic Manufacturing Co.

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Devices
14

What Ace Orthopedic Manufacturing Co. makes

Ace Orthopedic Manufacturing Co. produces orthopedic fixation devices, including external fixation systems like the ACE Fischer External Fixation Device and unilateral fixators, as well as intramedullary nails such as the AIM Suprcondylar Nail and ACE Humeral Nail. Their portfolio also includes self-drilling threaded pins, bone clamps, distraction bars, and captured hip screws for fracture stabilization. Surgical tools like the Trippi-Wells Dual Purpose Universal Tong and external articulation components are part of their offerings. Additionally, they manufacture specialized medical syringes, such as anal/rectal syringes, for clinical use.

The company’s devices are classified under FDA categories, including Class I and Class II, with submissions supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

Catalogue14

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  • Ace Fischer External Fixation Device Ref K801594

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

  • Trippi-Wells Dual Purpose Universal Tong Ref K810193

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

  • Anal/Rectal Syringe Ref K761229

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

  • Aim Supracondylar Nail Ref K934962

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

  • Threaded Pin, Self Drilling Ref K781251

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

  • Ace External Bone Clamp Part #S11 Ref K791466

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

  • Ace/Kyle Captured Hip Screw Ref K813554

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

  • External Articulation Ref K781840

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

  • Ace Humeral Nail Ref K934643

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

  • Bone Clamp, Ace External Ref K781839

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

  • Bar, Distraction Ref K781841

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

  • Ace Unilateral Fixator Ii Ref K936045

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

  • Ace 100 Degrees Tubular Plate Ref K920738

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

  • Ace 8.0mm Cannulated Cancellous Bone Screw Ref K926047

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

Rows 1-14 of 14

Frequently asked questions

How many devices does Ace Orthopedic Manufacturing Co. have in the registry?

The registry currently lists 14 devices for Ace Orthopedic Manufacturing Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ace Orthopedic Manufacturing Co.'s devices?

Among its 14 most recently registered devices, Ace Orthopedic Manufacturing Co. has devices listed in FDA 510(k) (14 devices).

What risk classes do Ace Orthopedic Manufacturing Co.'s devices fall under?

Among its 14 most recently registered devices, the classes recorded for Ace Orthopedic Manufacturing Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ace Orthopedic Manufacturing Co. in the registry?

The most recently registered devices listed for Ace Orthopedic Manufacturing Co. include ACE FISCHER EXTERNAL FIXATION DEVICE, TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG, ANAL/RECTAL SYRINGE and AIM SUPRACONDYLAR NAIL.

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