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Data / Medical devices / United States / Totalskincare.com, LLC

Totalskincare.com, LLC: FDA-registered device maker in Rockville, MD, United States, 1 510(k) clearance

Totalskincare.com, LLC is registered with the FDA (registration 3022076670) in Rockville, MD, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 27, 2005. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3022076670
Address
11910 Parklawn Dr Ste U, Rockville, MD, United States, 20852
Owner or operator
Kit U Safe Nala, LLC (10084728)
Roles
Repackager or relabeler
First device listed
March 25, 2022
Registered through
2026
Brand names listed
Kit U Safe Feminine Hygiene Kit

Devices it lists

DeviceProduct codeClassRoleSource
Pad, Menstrual, UnscentedHHD1Repackager or relabeleraccessdata.fda.gov
Tampon, Menstrual, UnscentedHEB2Repackager 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
December 27, 2005K051290TAMPAX PEARL PLASTIC APPLICATOR TAMPONS, ULTRA ABSORBENCY (UNSCENTED AND SCENTED)HEBSubstantially EquivalentProcter & Gamble Co.accessdata.fda.gov

Compare with other makers

Updated December 27, 2005. 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.