Data / Medical devices / United States / WOO More Play

WOO More Play: FDA-registered device maker in West Hollywood, CA, United States, 1 510(k) clearance

WOO More Play is registered with the FDA (registration 3030155386) in West Hollywood, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 1, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3030155386

Address

750 N. San Vicente Blvd. Suite 1075, West Hollywood, CA, United States, 90069

Owner or operator

Woo Essentials, Inc. (10089574)

Roles

Complaint file establishment, Specification developer

First device listed

December 19, 2023

Registered through

2026

Brand names listed

Coconut Love Oil

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.

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Updated December 1, 2023. 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.