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Teknar, Inc.

United StatesFDA applicant, unverified

Devices
18

What Teknar, Inc. makes

Teknar, Inc. manufactures ophthalmic ultrasound devices such as the OPHTHASONIC A-SCAN, OPHTHASONIC A-SCAN/B-SCAN, OPHTHASONIC A/P III, and B-SCAN 10 MHZ PROBE, as well as biopsy tools like the PRO-CUT BIOPSY NEEDLE and related accessories including the TEKNAR PROSCAN(TM) and TEKNAR PROSCAN ACCESSORY PROBE. The company also produces general medical support devices such as the IV STAND and FISCH DRILL PUMP, along with diagnostic units like the VC III, AXISONIC II, and BETASONIC III.

Teknar, Inc.'s devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 24 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue18

Newest first, rows 1-18 of 18

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  • Vc Iii Ref K823011

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

  • Teknar Proscan(Tm) Ref K864807

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

  • Pro-Cut Biopsy Needle Ref K891777

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

  • Ophthasonic A-Scan Ref K860757

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

  • Teknar Proscan Accessory Probe Ref K880659

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

  • Ophthasonic A-Scan/ B-Scan Ref K871536

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

  • Axisonic Ii Ref K810697

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

  • Fisch Drill Pump Ref K822900

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

  • Ophthasonic A/P Iii Ref K903666

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

  • B-Scan 10 Mhz Probe Ref K896038

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

  • Iv Stand Ref K830474

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

  • Betasonic Iii Ref K850116

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

  • Axipac Ii Ref K834539

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

  • Teknar Percu-Scan Ref K881850

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

  • Image 2000 System, Imaging, Ultra-Sonic Ref K896150

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

  • Biopsy Guide Ref K881605

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

  • Vocon Model VC526 Ref K801314

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

  • Probe, Imaging, Ultrasonic, Mechanical Sector Ref K883965

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

Rows 1-18 of 18

Frequently asked questions

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

The registry currently lists 18 devices for Teknar, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Teknar, Inc.'s devices?

Among its 18 most recently registered devices, Teknar, Inc. has devices listed in FDA 510(k) (18 devices).

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

Among its 18 most recently registered devices, the classes recorded for Teknar, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Teknar, Inc. include VC III, TEKNAR PROSCAN(TM), PRO-CUT BIOPSY NEEDLE and OPHTHASONIC A-SCAN.

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