Data / Medical devices / United States / Currie Medical, Inc.
Currie Medical, Inc.: FDA-registered device maker in Norfolk, VA, United States, 1 510(k) clearance
Currie Medical, Inc. is registered with the FDA (registration 3030063003) in Norfolk, VA, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 14, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3030063003
- Address
- 3701 East Virginia Beach, Norfolk, VA, United States, 23502
- Owner or operator
- Currie Medical, Inc. (10085857)
- Roles
- Contract manufacturer, Manufacturer, Remanufacturer, Specification developer
- First device listed
- March 20, 2023
- Registered through
- 2026
- Brand names listed
- ALP 900, Northfield Medical Manufacturing
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Drape, Surgical, Exempt | PUI | 2 | Contract manufacturer, Manufacturer, Specification developer | accessdata.fda.gov |
| Freezer | JRM | 1 | Manufacturer, Remanufacturer, Specification developer | accessdata.fda.gov |
| Sleeve, Limb, Compressible | JOW | 2 | Specification developer | accessdata.fda.gov |
| Warmer, Irrigation Solution | LHC | 1 | Manufacturer, Remanufacturer, 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 |
|---|---|---|---|---|---|---|
| December 14, 2023 | K231801 | MedHealth DVT compression Devices MHH900S/MHH900E | JOW | Substantially Equivalent | Medhealth Medical Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Drape, Surgical, Exempt
- All makers of Sleeve, Limb, Compressible
- All makers of Freezer
- All makers of Warmer, Irrigation Solution
Updated December 14, 2023. 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.