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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 101-150 of 847

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  • N/A CC940-25

    None Registry: GUDID Class:I
  • N/A Sm-4011S1

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  • N/A H-145

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  • N/A Agc-020

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  • N/A Ors-300

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  • N/A Ptr-3245-02R

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  • N/A Zm-171

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  • N/A Sm-4051

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  • N/A H-124

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  • N/A A2070

    None Registry: GUDID Class:I
  • N/A Sy-905

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  • N/A Oos-825

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  • N/A Zh-260

    None Registry: GUDID Class:I
  • N/A Mb-12013

    None Registry: GUDID Class:I
  • N/A Agc-105

    None Registry: GUDID Class:I
  • N/A Old-800004

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  • N/A Sm-3414

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  • N/A H-330

    None Registry: GUDID Class:I
  • N/A Sm-1414

    None Registry: GUDID Class:I
  • N/A L1670

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  • N/A Sm-3051

    None Registry: GUDID Class:I
  • N/A Zh-056

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  • N/A H-258

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  • N/A Oos-889

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  • N/A Mb-17009

    None Registry: GUDID Class:I
  • N/A Sm-1416

    None Registry: GUDID Class:I
  • N/A R1070N

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  • N/A Oar-1821

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  • N/A R1870N

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  • N/A Oos-135

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  • N/A DX6-262

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  • N/A Dx-241

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  • N/A Oos-175

    None Registry: GUDID Class:I
  • N/A Zo-661

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  • N/A H-214

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  • N/A Ok-124

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  • N/A H-266

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  • N/A Zhs-272

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  • N/A MR10BA20D

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  • N/A Zms-4006

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  • N/A Zm-233

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  • N/A Zhs-530

    None Registry: GUDID Class:I
  • N/A Zm-237

    None Registry: GUDID Class:I
  • N/A X-21554

    None Registry: GUDID Class:I
  • N/A L1670N

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  • N/A Agc-553

    None Registry: GUDID Class:I
  • N/A Oos-6134

    None Registry: GUDID Class:I
  • N/A Oos-860

    None Registry: GUDID Class:I
  • N/A Dx-222

    None Registry: GUDID Class:I
  • N/A Ors-028

    None Registry: GUDID Class:I

Rows 101-150 of 847

Showing 101-150 of 847

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.