Data / Medical devices / United States / Playground For All

Playground For All: FDA-registered device maker in San Francisco, CA, United States, 1 510(k) clearance

Playground For All is registered with the FDA (registration 3029582965) in San Francisco, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 30, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3029582965

Address

4645 Califronia St, San Francisco, CA, United States, 94118

Owner or operator

Playground For All (10088865)

Roles

Specification developer

First device listed

October 17, 2023

Registered through

2026

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 January 30, 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.