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Karlin Technology, Inc.

United StatesFDA applicant, unverified

Devices
17

What Karlin Technology, Inc. makes

Karlin Technology, Inc. manufactures a range of surgical instruments including crank frame retractors, suction retractors (including tower‑attach versions), spinal distractors and spanners, Cobb spinal elevators, lumbar impact sets and bone graft impactors, self‑retaining soft tissue retractors, bone screws, X‑ray markers, microdiscectomy and orthopedic/spinal ring curettes, and a universally adjustable armboard.

The devices are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) database. Karlin Technology, Inc. is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue17

Newest first, rows 1-17 of 17

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  • Crank Frame Retractor Ref K882071

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

  • Suction Retractors Ref K882074

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

  • Spinal Distractors, Spanners Ref K882069

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

  • Cobb Spinal Elevators Ref K882068

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

  • Lumbar Impaction Set And Bone Graft Impactors Ref K882070

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

  • Self-Retaining Soft Tissue Retractor Ref K882075

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

  • Suction Retractor(Tower Attach.)For Crank Fram Ret Ref K903969

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

  • Bone Screw Ref K893203

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

  • X-Ray Marker Ref K882519

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

  • Microdiscectomy Currettes Ref K882077

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

  • Orthopaedic And Spinal Ring Currettes Ref K882072

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

  • Universally Adjustable Armboard Ref K882524

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

  • Spinal Microknife Ref K882525

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

  • Shoulder Bolster, Knee, Ankle & Leg Support Pads Ref K882520

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

  • Spinal Surgery Frame Ref K882078

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

  • Bone Plate Ref K893201

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

  • Spinal Needle Ref K882073

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

Rows 1-17 of 17

Frequently asked questions

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

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

Which registries list Karlin Technology, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Karlin Technology, Inc. include CRANK FRAME RETRACTOR, SUCTION RETRACTORS, SPINAL DISTRACTORS, SPANNERS and COBB SPINAL ELEVATORS.

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