Data / Medical devices / United States / King Brand Healthcare Products
King Brand Healthcare Products: FDA-registered device maker in Bellingham, WA, United States, 1 510(k) clearance
King Brand Healthcare Products is registered with the FDA (registration 3012639937) in Bellingham, WA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 17, 1981. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3012639937
- Address
- 1325 Meador Ave, Bellingham, WA, United States, 98229
- Owner or operator
- King Brand Healthcare Products (10032716)
- Roles
- Manufacturer, Specification developer
- First device listed
- August 3, 2010
- Registered through
- 2026
- Brand names listed
- BFST, Ceanix, ColdCure, Energy Web, Freezie, Inferno Wrap, KB Tape, KBTech and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Elastic | FQM | 1 | Specification developer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Manufacturer | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 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 |
|---|---|---|---|---|---|---|
| February 17, 1981 | K810137 | SOF-BAND HIGH STRETCH BANDAGES | FQM | Substantially Equivalent | Johnson & Johnson Professionals, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Bandage, Elastic
- All makers of Pad, Heating, Powered
- All makers of Pack, Hot Or Cold, Reusable
Updated February 17, 1981. 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.