Data / Medical devices / United States / Bright Supply Inc
Bright Supply Inc: FDA-registered device maker in Canoga Park, CA, United States, 2 510(k) clearances
Bright Supply Inc is registered with the FDA (registration 3017498782) in Canoga Park, CA, United States. It lists 29 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 25, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017498782
- Address
- 7849 Canoga Ave, Canoga Park, CA, United States, 91304
- Owner or operator
- Bright Supply Inc (10078145)
- Roles
- Complaint file establishment
- First device listed
- October 12, 2020
- Registered through
- 2026
- Brand names listed
- Britedent
Devices it lists
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 25, 2022 | K220512 | Disposable Surgical Face Mask (M01, M02) | FXX | Substantially Equivalent | Fomed Industries, Inc. | accessdata.fda.gov |
| September 9, 2015 | K143637 | U&U Sterilization Pouch and Roll | FRG | Substantially Equivalent | U&U Medical Technology Co, Ltd. | accessdata.fda.gov |
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Updated April 25, 2022. 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.