Data / Medical devices / United States / Oral-B Laboratories
Oral-B Laboratories: FDA-registered device maker in Iowa City, IA, United States, 1 510(k) clearance
Oral-B Laboratories is registered with the FDA (registration 3013646822) in Iowa City, IA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 31, 2006. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3013646822
- Address
- 1375 Highway 1 W, Iowa City, IA, United States, 52246
- Owner or operator
- Procter & Gamble (9915005)
- Roles
- Manufacturer
- First device listed
- December 6, 2007
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Toothbrush, Powered | JEQ | 1 | 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 |
|---|---|---|---|---|---|---|
| May 31, 2006 | K061199 | ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES | JEQ | Substantially Equivalent | Braun GmbH | accessdata.fda.gov |
Compare with other makers
Updated May 31, 2006. 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.