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Gottfried Medical, Inc.

Also registered as Gotfried Medical, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1526072

Devices
147
Registrations
FDA
FDA recalls
0

What Gottfried Medical, Inc. makes

Gottfried Medical, Inc. manufactures reusable compression garments, including pressure shirts, pants, socks, stockings, gloves, and scar-management dressings. Their product line also includes scrotal support devices designed to provide targeted pressure for medical or post-surgical use.

The company’s devices are classified as Class I or Class II under FDA regulations and are listed via 510(k) clearance and the FDA’s Unique Device Identification (UDI) system. These products are intended for use in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue147

Newest first, rows 1-50 of 147

Search and filter all 147 devices
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  • Compression Stocking 021

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 022

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 101

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 102

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 104

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 103

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 106

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 201

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 202

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 300

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 301

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 302

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 305

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 303

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 304

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 306

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 308

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 307

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 309

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 331

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 332

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 334

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 333

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 335

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 339

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 336

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 338

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 337

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 341

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 342

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 400

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 401

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 402

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 403

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 404

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 405

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 407

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 406

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 408

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 409

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 410

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 412

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 413

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Compression Stocking 414

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 415

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 416

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 417

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 418

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 420

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Compression Stocking 421

    Active Regimes: 510(k) Registry: GUDID Class:I

Rows 1-50 of 147

Showing 1-50 of 147

Company details

FDA FEI number
1526072
Address
2920 Centennial Rd, Toledo, OH, 43617

Frequently asked questions

How many devices does GOTTFRIED MEDICAL, INC. have in the registry?

The registry currently lists 147 devices for GOTTFRIED MEDICAL, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list GOTTFRIED MEDICAL, INC.'s devices?

Among its 50 most recently registered devices, GOTTFRIED MEDICAL, INC. has devices listed in FDA GUDID (50 devices).

What risk classes do GOTTFRIED MEDICAL, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for GOTTFRIED MEDICAL, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from GOTTFRIED MEDICAL, INC. in the registry?

The most recently registered devices listed for GOTTFRIED MEDICAL, INC. include Compression Stocking 021, Compression Stocking 022, Compression Stocking 101 and Compression Stocking 102.

Generated automatically from registry data and not verified by a human reviewer.

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