Data / Medical devices / United States / Bossong Hosiery Mills
Bossong Hosiery Mills: FDA-registered device maker in Asheboro, NC, United States, 1 510(k) clearance
Bossong Hosiery Mills is registered with the FDA (registration 3002960458) in Asheboro, NC, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 2, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002960458
- Address
- 840 W Salisbury St, Asheboro, NC, United States, 27203
- Owner or operator
- Bossong Hosiery Mills (10044067)
- Roles
- Manufacturer
- First device listed
- April 25, 2013
- Registered through
- 2026
- Brand names listed
- Bossong Hosiery Compression Stockings, Plantars Fasciitis compression brace
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Joint, Ankle, External Brace | ITW | 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 |
|---|---|---|---|---|---|---|
| April 2, 2013 | K123820 | BOSSONG HOSIERY MEDICAL COMPRESSION STOCKINGS 8-15 MMHG, BOSSONG HOSIERY ANTI-EMBOLISM STOCKINGS 10-20 MMHG, BOSSONG HOS | DWL | Substantially Equivalent | Bossong Hosiery Mills, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
- All makers of Joint, Ankle, External Brace
- All makers of Stocking, Medical Support (For General Medical Purposes)
Updated April 2, 2013. 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.