Data / Medical devices / United States / Medipurpose, Inc.
Medipurpose, Inc.: FDA-registered device maker in Duluth, GA, United States, 1 510(k) clearance
Medipurpose, Inc. is registered with the FDA (registration 1066648) in Duluth, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 1, 2011. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1066648
- FEI number
- 3003244344
- Address
- 2862 Buford Hwy Ste 105, Duluth, GA, United States, 30096
- Owner or operator
- MediPurpose, Inc (9045381)
- Roles
- Specification developer
- First device listed
- October 8, 2026
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | Specification developer | 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 |
|---|---|---|---|---|---|---|
| September 1, 2011 | K110062 | MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG | FRO | Substantially Equivalent | Medipurpose Pte. , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 1, 2011. 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.