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Data / Medical devices / United States / J&J Distributors

J&J Distributors: FDA-registered device maker in Lakewood, NJ, United States, 1 510(k) clearance

J&J Distributors is registered with the FDA (registration 3015825358) in Lakewood, NJ, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 31, 2006. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3015825358
Address
479 Oberlin Ave South Lakewood NJ 08701 Unit 303 Office-198 Glen Ave South Lakewood, NJ 08701, Lakewood, NJ, United States, 08701
Owner or operator
J&J Distributors (10077946)
Roles
Repackager or relabeler
First device listed
March 11, 2021
Registered through
2026
Brand names listed
J&J DIstributors, Oral B Toothbrush

Devices it lists

DeviceProduct codeClassRoleSource
Culture Media, Non-Selective And Non-DifferentialJSG1Repackager or relabeleraccessdata.fda.gov
Toothbrush, PoweredJEQ1Repackager or relabeleraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 31, 2006K061199ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIESJEQSubstantially EquivalentBraun GmbHaccessdata.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.