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Omega Surgical Instruments, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1000220740

Devices
847
Registrations
FDA
FDA recalls
0

What Omega Surgical Instruments, Inc. makes

Omega Surgical Instruments, Inc. manufactures orthopedic fixation devices, including K-wires and Steinmann pins for bone stabilization, as well as surgical tools such as general and plastic surgery bur instruments and saw blades for bone or tissue cutting.

The company’s portfolio includes Class I and Class II devices, with products listed under the FDA’s 510(k) clearance process. The manufacturer is based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue847

Newest first, rows 51-100 of 847

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  • N/A Zm-230

    None Registry: GUDID Class:I

  • N/A S4070

    None Registry: GUDID Class:I

  • N/A Sm-4040

    None Registry: GUDID Class:I

  • N/A Zo-619

    None Registry: GUDID Class:I

  • N/A MR9BA40

    None Registry: GUDID Class:I

  • N/A R4570N

    None Registry: GUDID Class:I

  • N/A Zo-684

    None Registry: GUDID Class:I

  • N/A X-27653

    None Registry: GUDID Class:I

  • N/A Oos-134

    None Registry: GUDID Class:I

  • N/A Sn-5804

    None Registry: GUDID Class:I

  • N/A Sm-3102

    None Registry: GUDID Class:I

  • N/A Zm-262

    None Registry: GUDID Class:I

  • N/A Sm-4513

    None Registry: GUDID Class:I

  • N/A S702L-51

    None Registry: GUDID Class:I

  • N/A Mb-12019

    None Registry: GUDID Class:I

  • N/A Om-1619

    None Registry: GUDID Class:I

  • N/A Oa-135

    None Registry: GUDID Class:I

  • N/A Zh-550

    None Registry: GUDID Class:I

  • N/A R3070

    None Registry: GUDID Class:I

  • N/A Orst-233

    None Registry: GUDID Class:I

  • N/A Omm-8501

    None Registry: GUDID Class:I

  • N/A Dxs-209

    None Registry: GUDID Class:I

  • N/A CC2-5X

    None Registry: GUDID Class:I

  • N/A CC940-23

    None Registry: GUDID Class:I

  • N/A Zm-260

    None Registry: GUDID Class:I

  • N/A S701-51

    None Registry: GUDID Class:I

  • N/A Ss-002

    None Registry: GUDID Class:I

  • N/A Zo-652

    None Registry: GUDID Class:I

  • N/A MR10BA30

    None Registry: GUDID Class:I

  • N/A Ozd-623

    None Registry: GUDID Class:I

  • N/A Zhs-1101

    None Registry: GUDID Class:I

  • N/A Omm-8201

    None Registry: GUDID Class:I

  • N/A Oos-6150

    None Registry: GUDID Class:I

  • N/A H-158

    None Registry: GUDID Class:I

  • N/A S1703L-51

    None Registry: GUDID Class:I

  • N/A X-21568

    None Registry: GUDID Class:I

  • N/A A3070

    None Registry: GUDID Class:I

  • N/A R6-60-01NS

    None Registry: GUDID Class:I

  • N/A Oos-831

    None Registry: GUDID Class:I

  • N/A Osd-819

    None Registry: GUDID Class:I

  • N/A H-358

    None Registry: GUDID Class:I

  • N/A Op-514

    None Registry: GUDID Class:I

  • N/A Sm-4105

    None Registry: GUDID Class:I

  • N/A R1570N

    None Registry: GUDID Class:I

  • N/A Zh-90119

    None Registry: GUDID Class:I

  • N/A W1051

    None Registry: GUDID Class:I

  • N/A Zm-238

    None Registry: GUDID Class:I

  • N/A Sm-4106

    None Registry: GUDID Class:I

  • N/A R60-51

    None Registry: GUDID Class:I

  • N/A Oos-897

    None Registry: GUDID Class:I

Rows 51-100 of 847

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Company details

FDA FEI number
1000220740
Address
1072 S. Elms Road, Flint, MI, 48532

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