Data / Medical devices / United States / Gottfried Medical, Inc.
Gottfried Medical, Inc.: FDA-registered device maker in Toledo, OH, United States, 2 510(k) clearances
Gottfried Medical, Inc. is registered with the FDA (registration 1526072) in Toledo, OH, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 30, 2001. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1526072
- Address
- 2920 Centennial Rd, Toledo, OH, United States, 43617
- Owner or operator
- GOTTFRIED MEDICAL, INC. (1526072)
- Roles
- Manufacturer
- First device listed
- July 6, 1992
- Registered through
- 2027
- Brand names listed
- Gottfried Medical, Gottfried Medical Made to Measure compression stockings, Gottfried Medical support for general medical purposes
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Elastomer, Silicone, For Scar Management | MDA | 1 | Manufacturer | accessdata.fda.gov |
| Stocking, Medical Support (For General Medical Purposes) | FQL | 1 | Manufacturer | accessdata.fda.gov |
| Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) | DWL | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 30, 2001 | K010675 | ENSIL FABRIC | MDA | Substantially Equivalent | Gottfried Medical, Inc. | accessdata.fda.gov |
| January 12, 1983 | K823737 | MADE-TO-MEASURE SURGICAL ELASTIC SUPPORT | DWL | Substantially Equivalent | Gotfried Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
- All makers of Elastomer, Silicone, For Scar Management
- All makers of Stocking, Medical Support (For General Medical Purposes)
Updated May 30, 2001. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.