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Playground For All

United Statesfrom the FDA registration address FDA establishment FEI 3029582965

Devices
1
Registrations
FDA
FDA recalls
0

What Playground For All makes

Playground For All designs and manufactures the Love Sesh, a sensory-friendly swing designed for individuals with autism or sensory processing needs, incorporating adjustable tension and motion controls for customised comfort and engagement.

The Love Sesh is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Playground For All Love Sesh Ref K222567

    Active Regimes: 510(k) Registry: 510(k) Class:II

Company details

FDA FEI number
3029582965
Address
4645 Califronia St, San Francisco, CA, 94118

Frequently asked questions

How many devices does Playground For All have in the registry?

The registry currently lists 1 device for Playground For All. Devices recorded under merged duplicate company entries are counted once.

Which registries list Playground For All's devices?

Among its 1 most recently registered device, Playground For All has devices listed in FDA 510(k) (1 device).

What risk classes do Playground For All's devices fall under?

Among its 1 most recently registered device, the classes recorded for Playground For All's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Playground For All in the registry?

The most recently registered devices listed for Playground For All include Playground For All Love Sesh.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.