Data / Medical devices / United States / B&B Molded Products
B&B Molded Products: FDA-registered device maker in Defiance, OH, United States, 1 510(k) clearance
B&B Molded Products is registered with the FDA (registration 3012736230) in Defiance, OH, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 14, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012736230
- Address
- 1250 Ottawa Ave., Defiance, OH, United States, 43512
- Owner or operator
- B&B Molded Products (10052524)
- Roles
- Repackager or relabeler
- First device listed
- August 10, 2016
- Registered through
- 2026
- Brand names listed
- Naturelle
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pad, Menstrual, Unscented | HHD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| July 14, 2003 | K031067 | FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS | HEB | Substantially Equivalent | First Quality Hygienic, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 14, 2003. 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.