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Data / Medical devices / United States / Ecochem Inc. Dba Wiser Living

Ecochem Inc. Dba Wiser Living: FDA-registered device maker in Paramount, CA, United States, 1 510(k) clearance

Ecochem Inc. Dba Wiser Living is registered with the FDA (registration 3011336685) in Paramount, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 30, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3011336685
Address
14733 1/2 Garfield Ave., Paramount, CA, United States, 90723
Owner or operator
ECOCHEM INC. DBA WISER LIVING (10086808)
Roles
Repackager or relabeler
First device listed
March 14, 2024
Registered through
2026
Brand names listed
Hair Boom Air, HairBoom

Devices it lists

DeviceProduct codeClassRoleSource
Lamp, Infrared, Therapeutic HeatingILY2Repackager or relabeleraccessdata.fda.gov
Laser, Comb, HairOAP2Repackager 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
September 30, 2019K192425Hair Boom 69, Hair Boom Air, Ulike Hair UpUpOAPSubstantially EquivalentWontech Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 30, 2019. 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.