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Surgical Technologies, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 2183319

Devices
28
Registrations
FDA
FDA recalls
0

What Surgical Technologies, Inc. makes

Surgical Technologies, Inc. makes surgical instruments and ophthalmic devices, including blunt dissecting scissors, tissue manipulators, aspirating endo ocular probes, I/A handpieces with replaceable tips, arthrogram trays, flexible biopsy cup forceps, cystoscopes, and related tools such as Babcock forceps, grasping forceps, needle holders, and bare-fiber endoilluminators.

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

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue28

Newest first, rows 1-28 of 28

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  • Blunt Dissecting Scissors Ref K930464

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

  • Surgical Technologies, Inc. Syringe Ref K951918

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

  • Sti Tissue Manipulator Ref K911699

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

  • Aspirating Endo Ocular Probe Ref K930123

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

  • I/A Handpiece With Replaceable Tips Ref K910245

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

  • Arthrogram Tray Ref K950683

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

  • Infinitech Soft Tip Flute Needle Ref K946181

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

  • Babcock Forceps, Grasping Forceps, Needle Holder Ref K930467

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

  • Aspirating Endo Ocular Probe Ref K914247

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

  • Bare-Fiber Endoilluminator Ref K933208

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

  • Flexible Biopsy Cup Forceps Ref K941158

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

  • Cystoscope Ref K941992

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

  • Locking Pivotal Thoracoport Ref K930463

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

  • Infinitech Aspirating Laser Probe Ref K946135

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

  • Biopsy Cup Forceps Ref K930180

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

  • Flexible Grasping Forceps Ref K941161

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

  • Oscilflator Ref K952566

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

  • Arthroscope Ref K942029

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

  • Compression Clamp Ref K930466

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

  • Biopsy Scissors Ref K942030

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

  • Wire Guided Oval Dilators Ref K930465

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

  • Disposable Irrigating/Aspirating Handpiece Ref K910973

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

  • Endoscopic Umbrella Retractor Ref K930462

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

  • Aspirating Endo Ocular Probe W/Illumination Ref K921488

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

  • Pressure Monitoring Extension Ref K942482

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

  • Surg Tech, Inc. 30 Gauge Straight Extrusion Needles Ref K910036

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

  • Infinitech Lighted Infusion Cannula Ref K946136

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

  • Thoracoscope/Laparoscope Ref K931954

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

Rows 1-28 of 28

Company details

FDA FEI number
2183319
Address
292 EAST LAFAYETTE FRONTAGE RD, ST. PAUL, MN, 55107

Frequently asked questions

How many devices does SURGICAL TECHNOLOGIES, INC. have in the registry?

The registry currently lists 28 devices for SURGICAL TECHNOLOGIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list SURGICAL TECHNOLOGIES, INC.'s devices?

Among its 28 most recently registered devices, SURGICAL TECHNOLOGIES, INC. has devices listed in FDA 510(k) (28 devices).

What risk classes do SURGICAL TECHNOLOGIES, INC.'s devices fall under?

Among its 28 most recently registered devices, the classes recorded for SURGICAL TECHNOLOGIES, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from SURGICAL TECHNOLOGIES, INC. in the registry?

The most recently registered devices listed for SURGICAL TECHNOLOGIES, INC. include BLUNT DISSECTING SCISSORS, SURGICAL TECHNOLOGIES, INC. SYRINGE, STI TISSUE MANIPULATOR and ASPIRATING ENDO OCULAR PROBE.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.