Data / Medical devices / United States / BSN medical inc.
BSN medical inc.: FDA-registered device maker in Hickory, NC, United States, 1 510(k) clearance
BSN medical inc. is registered with the FDA (registration 1043537) in Hickory, NC, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 4, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1043537
- Address
- 1555 4th Ave SE, Hickory, NC, United States, 28602
- Owner or operator
- BSN medical GmbH (9047426)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 14, 2003
- Registered through
- 2026
- Brand names listed
- AO Cast Saw, AO Cast Vacuum, Actimove Everyday Supports Posture Control Brace, Delta-Cast Saw, Delta-Cast Serene Cast Remover, Delta-Cast Vacuum, Epstein Facioplasty, FLA Muscle Support and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Binder, Medical, Therapeutic | MDR | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Cast Removal, Ac-Powered | LGH | 1 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| April 4, 1994 | K925154 | JOBST-CUSTOM | DWL | Substantially Equivalent | Jobst Institute, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Binder, Medical, Therapeutic
- All makers of Instrument, Cast Removal, Ac-Powered
- All makers of Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
Updated April 4, 1994. 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.