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Data / Medical devices / United States / PR Personal Care Laboratories

PR Personal Care Laboratories: FDA-registered device maker in Santa Clarita, CA, United States, 1 510(k) clearance

PR Personal Care Laboratories is registered with the FDA (registration 3012112573) in Santa Clarita, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 11, 2026. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3012112573
Address
27820 Fremont Court Suite 3, Santa Clarita, CA, United States, 91355
Owner or operator
PR Personal Care Laboratories (10085919)
Roles
Contract manufacturer, Manufacturer
First device listed
September 8, 2022
Registered through
2027
Brand names listed
PR Water-Base Lube Personal Lubricant

Devices it lists

DeviceProduct codeClassRoleSource
Lubricant, PersonalNUC2Contract manufacturer, Manufactureraccessdata.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
June 11, 2026K261292PR Water-Base Lube Personal Lubricant (PR Water-Base Lube Personal Lubricant)NUCSubstantially EquivalentPR Personal Care Laboratoriesaccessdata.fda.gov

Compare with other makers

Updated June 11, 2026. 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.