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O Co., Inc.

United StatesFDA 510(k) applicant, unverified

Devices
17

What O Co., Inc. makes

O Co., Inc. manufactures dental implant components, including endosseous dental implants, abutments (standard and healing), implant body retrievers/removers, parallel pins, and accessories like depth gauges and immediate stabilizing devices. Their portfolio also covers custom-diameter implants (e.g., 5.0mm) and additional attachment items for endosseous implants.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company’s products are listed in the FDA’s 510(k) registry, adhering to U.S. medical device compliance standards.

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

Catalogue17

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  • Oco Dental Implant Ref K010142

    Class II
    Active 510(k) 510(k) II

  • O Butment Et Implant Ref K961665

    Class II
    Active 510(k) 510(k) II

  • Implant Body Retriever/Remover Ref K946113

    Class II
    Active 510(k) 510(k) II

  • Parrallel Pin Ref K944904

    Class II
    Active 510(k) 510(k) II

  • Oco Dental Implant Ref K021460

    Class II
    Active 510(k) 510(k) II

  • Oco Dental Implant (5.0mm Diameter) Ref K023336

    Class II
    Active 510(k) 510(k) II

  • Accessory Item To Endosseous Dental Implant Ref K945300

    Class II
    Active 510(k) 510(k) II

  • Dental Implant Endosseous Ref K950066

    Class II
    Active 510(k) 510(k) II

  • Immediate Stabilizing Device (Isd) Ref K011524

    Class II
    Active 510(k) 510(k) II

  • O Butment Ref K903211

    Class II
    Active 510(k) 510(k) II

  • O Butment Hb Ref K921933

    Class II
    Active 510(k) 510(k) II

  • Implant Body Depth Gauge/Tryin Ref K946129

    Class II
    Active 510(k) 510(k) II

  • Obutment Hb Ref K903999

    Class II
    Active 510(k) 510(k) II

  • O Butment Es Implant Ref K923889

    Class II
    Active 510(k) 510(k) II

  • O Butment Ref K884296

    Class II
    Active 510(k) 510(k) II

  • Immediate Stabilizing Implant (Isi) Ref K033392

    Class II
    Active 510(k) 510(k) II

  • O Butment Hs Implant Ref K973926

    Class II
    Active 510(k) 510(k) II

Rows 1-17 of 17

Frequently asked questions

How many devices does O Co., Inc. have in the registry?

The registry currently lists 17 devices for O Co., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list O Co., Inc.'s devices?

Among its 17 most recently registered devices, O Co., Inc. has devices listed in FDA 510(k) (17 devices).

What risk classes do O Co., Inc.'s devices fall under?

Among its 17 most recently registered devices, the classes recorded for O Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from O Co., Inc. in the registry?

The most recently registered devices listed for O Co., Inc. include OCO DENTAL IMPLANT, O BUTMENT ET IMPLANT, IMPLANT BODY RETRIEVER/REMOVER and PARRALLEL PIN.

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