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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 501-550 of 847

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  • N/A Sm-3114

    None Registry: GUDID Class:I

  • N/A H-368

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  • N/A Sm-4115

    None Registry: GUDID Class:I

  • N/A Ok-135

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  • N/A Es-MH30

    None Registry: GUDID Class:I

  • N/A Ok-154

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  • N/A Ptr-3230-02R

    None Registry: GUDID Class:I

  • N/A S5070

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  • N/A D4070

    None Registry: GUDID Class:I

  • N/A R1870

    None Registry: GUDID Class:I

  • N/A Od-412

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  • N/A Ors-101NS

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  • N/A Zms-4011

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  • N/A Zh-555

    None Registry: GUDID Class:I

  • N/A Sm-3411

    None Registry: GUDID Class:I

  • N/A Zhs-205

    None Registry: GUDID Class:I

  • N/A MR9BA30D

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  • N/A ROPS2050

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  • N/A Dx-224

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  • N/A Ors-720

    None Registry: GUDID Class:I

  • N/A Zo-644

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  • N/A D3570N

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  • N/A S699-51

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  • N/A DX6-266

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  • N/A H-320

    None Registry: GUDID Class:I

  • N/A Zm-231

    None Registry: GUDID Class:I

  • N/A Ds-99001

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  • N/A Oos-820

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  • N/A Age-241

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  • N/A X-21570

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  • N/A Ok-149

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  • N/A H-168

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  • N/A Zm-233S-13

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  • N/A W2051

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  • N/A Oos-885

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  • N/A H-338

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  • N/A Zh-258

    None Registry: GUDID Class:I

  • N/A Ss-109

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  • N/A Ss-304

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  • N/A Sm-3108

    None Registry: GUDID Class:I

  • N/A Osd-8510

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  • N/A Ssm-048

    None Registry: GUDID Class:I

  • N/A S5070N

    None Registry: GUDID Class:I

  • N/A Agc-010

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  • N/A S560-51N

    None Registry: GUDID Class:I

  • N/A R8-60-01NS

    None Registry: GUDID Class:I

  • N/A Sm-1103

    None Registry: GUDID Class:I

  • N/A MR14MH30

    None Registry: GUDID Class:I

  • N/A Zhs-145

    None Registry: GUDID Class:I

  • N/A R6-51

    None Registry: GUDID Class:I

Rows 501-550 of 847

Showing 501-550 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.