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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 451-500 of 847

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  • N/A D1070N

    None Registry: GUDID Class:I

  • N/A Sm-6412

    None Registry: GUDID Class:I

  • N/A Sn-5805

    None Registry: GUDID Class:I

  • N/A Ok-133

    None Registry: GUDID Class:I

  • N/A Oa-566R

    None Registry: GUDID Class:I

  • N/A Zms-3058

    None Registry: GUDID Class:I

  • Na Sm-5009-01

    None Registry: GUDID Class:I

  • N/A H-362

    None Registry: GUDID Class:I

  • N/A Oos-803

    None Registry: GUDID Class:I

  • N/A S703L-51

    None Registry: GUDID Class:I

  • N/A Ok-155

    None Registry: GUDID Class:I

  • N/A Ozd-621

    None Registry: GUDID Class:I

  • N/A Oos-100

    None Registry: GUDID Class:I

  • N/A D2070

    None Registry: GUDID Class:I

  • N/A Sm-1102

    None Registry: GUDID Class:I

  • N/A D3070N

    None Registry: GUDID Class:I

  • N/A S702-51

    None Registry: GUDID Class:I

  • N/A H-122

    None Registry: GUDID Class:I

  • N/A Zms-3115

    None Registry: GUDID Class:I

  • N/A Zm-263

    None Registry: GUDID Class:I

  • N/A Zo-682

    None Registry: GUDID Class:I

  • N/A H-142

    None Registry: GUDID Class:I

  • N/A Zm-232

    None Registry: GUDID Class:I

  • N/A H-262

    None Registry: GUDID Class:I

  • N/A Ok-121

    None Registry: GUDID Class:I

  • N/A H-260

    None Registry: GUDID Class:I

  • N/A D6070

    None Registry: GUDID Class:I

  • N/A S702-60-01NS

    None Registry: GUDID Class:I

  • N/A O4035N

    None Registry: GUDID Class:I

  • N/A Zo-686

    None Registry: GUDID Class:I

  • N/A Zm-084B

    None Registry: GUDID Class:I

  • N/A R2070

    None Registry: GUDID Class:I

  • N/A Ol-195

    None Registry: GUDID Class:I

  • N/A CC2-0S

    None Registry: GUDID Class:I

  • N/A Ss-114

    None Registry: GUDID Class:I

  • N/A Mb-14001

    None Registry: GUDID Class:I

  • N/A Zm-053

    None Registry: GUDID Class:I

  • N/A Zh-259

    None Registry: GUDID Class:I

  • N/A Sm-3111

    None Registry: GUDID Class:I

  • N/A SH206508

    None Registry: GUDID Class:I

  • N/A Oos-855

    None Registry: GUDID Class:I

  • N/A Ok-132

    None Registry: GUDID Class:I

  • N/A Mb-12017

    None Registry: GUDID Class:I

  • N/A DX6-267

    None Registry: GUDID Class:I

  • N/A Zst-032

    None Registry: GUDID Class:I

  • N/A R2070N

    None Registry: GUDID Class:I

  • N/A O40-65-01NS

    None Registry: GUDID Class:I

  • N/A Sm-3809

    None Registry: GUDID Class:I

  • N/A H-401

    None Registry: GUDID Class:I

  • N/A S700-51N

    None Registry: GUDID Class:I

Rows 451-500 of 847

Showing 451-500 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.