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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 201-250 of 847

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  • N/A A5070

    None Registry: GUDID Class:I
  • N/A Agc-281

    None Registry: GUDID Class:I
  • N/A MR10BA20

    None Registry: GUDID Class:I
  • N/A R4070

    None Registry: GUDID Class:I
  • N/A Oos-875

    None Registry: GUDID Class:I
  • N/A Zh-577

    None Registry: GUDID Class:I
  • N/A Dx-266

    None Registry: GUDID Class:I
  • N/A Sm-1417

    None Registry: GUDID Class:I
  • N/A Sm-3514

    None Registry: GUDID Class:I
  • N/A Zo-648

    None Registry: GUDID Class:I
  • N/A Osd-844

    None Registry: GUDID Class:I
  • N/A X-21567

    None Registry: GUDID Class:I
  • N/A Zo-674

    None Registry: GUDID Class:I
  • N/A Zh-102

    None Registry: GUDID Class:I
  • N/A R3570

    None Registry: GUDID Class:I
  • N/A Ozd-624

    None Registry: GUDID Class:I
  • N/A Hc-186

    None Registry: GUDID Class:I
  • N/A Mb-12008

    None Registry: GUDID Class:I
  • N/A Oos-845

    None Registry: GUDID Class:I
  • N/A Oos-132

    None Registry: GUDID Class:I
  • N/A Op-510

    None Registry: GUDID Class:I
  • N/A Ozd-625

    None Registry: GUDID Class:I
  • N/A Zo-663

    None Registry: GUDID Class:I
  • N/A H-420

    None Registry: GUDID Class:I
  • N/A H-332

    None Registry: GUDID Class:I
  • N/A Ok-143

    None Registry: GUDID Class:I
  • N/A Osd-835

    None Registry: GUDID Class:I
  • N/A H-183

    None Registry: GUDID Class:I
  • N/A Mb-12011

    None Registry: GUDID Class:I
  • N/A Ok-134

    None Registry: GUDID Class:I
  • N/A Oos-856

    None Registry: GUDID Class:I
  • N/A Ol-124

    None Registry: GUDID Class:I
  • N/A R4570

    None Registry: GUDID Class:I
  • N/A Zo-667

    None Registry: GUDID Class:I
  • N/A Zo-646

    None Registry: GUDID Class:I
  • N/A H-164

    None Registry: GUDID Class:I
  • N/A H-422

    None Registry: GUDID Class:I
  • N/A H-322

    None Registry: GUDID Class:I
  • N/A MR9BA60

    None Registry: GUDID Class:I
  • N/A A3070N

    None Registry: GUDID Class:I
  • N/A Mb-12007

    None Registry: GUDID Class:I
  • N/A Od-410

    None Registry: GUDID Class:I
  • N/A Zh-261

    None Registry: GUDID Class:I
  • N/A Oos-844

    None Registry: GUDID Class:I
  • N/A Oos-150

    None Registry: GUDID Class:I
  • N/A Zh-203

    None Registry: GUDID Class:I
  • N/A R2770N

    None Registry: GUDID Class:I
  • N/A Sm-4006

    None Registry: GUDID Class:I
  • Na Sm-3809NS

    None Registry: GUDID Class:I
  • N/A Es-BA140

    None Registry: GUDID Class:I

Rows 201-250 of 847

Showing 201-250 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.