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Data / Medical devices / Pad, Menstrual, Unscented / United States

FDA-registered makers of Pad, Menstrual, Unscented in the United States: 30 establishments

30 establishments in the United States are registered with the FDA to make Pad, Menstrual, Unscented (product code HHD). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Pad, Menstrual, Unscented
Product code
HHD
Country
United States

Makers of Pad, Menstrual, Unscented in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Customed, Inc.Fajardo, PR, United StatesManufacturer3August 21, 1990000api.fda.gov
Advanced Concept Innovations LLCLakeland, FL, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Alg WW LLCRedmond, WA, United StatesSpecification developer0000api.fda.gov
Attends Healthcare ProductsGreenville, NC, United StatesSpecification developer0000api.fda.gov
Busse Hospital DisposablesHauppauge, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
COAM, Inc.Coppell, TX, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Drylock Technologies LtdEau Claire, WI, United StatesManufacturer0000api.fda.gov
Egal Pads Inc.Somerville, MA, United StatesSpecification developer0000api.fda.gov
Essity HMS North America Inc.Dover, DE, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Fischer Manufacturing LLCFairfield, OH, United StatesContract manufacturer0000api.fda.gov
First Quality Retail Services, LLCLewistown, PA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
FridaBaby LLCMiami, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Genial Day IncBolingbrook, IL, United StatesManufacturer0000api.fda.gov
GladRagsPortland, OR, United StatesManufacturer0000api.fda.gov
Health Care Products, Inc.Coldwater, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Hempress HygienicsWilmington, DE, United StatesSpecification developer0000api.fda.gov
Hospora IncIrvine, CA, United StatesSpecification developer0000api.fda.gov
Kimberly-Clark CorporationNeenah, WI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
KIMBERLY-CLARK CORPORATION Cold SpringNeenah, WI, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
MKJ Brands LLCHackensack, NJ, United StatesManufacturer0000api.fda.gov
Ontex Operations USA, LLCStokesdale, NC, United StatesContract manufacturer, Manufacturer0000api.fda.gov
P&G Paper Products Co. Box Elder PlantBear River City, UT, United StatesManufacturer0000api.fda.gov
Pixie Cup LLCWalnut Shade, MO, United StatesSpecification developer0000api.fda.gov
Pixie, Inc.New York, NY, United StatesSpecification developer0000api.fda.gov
Procter & Gamble Co.Cincinnati, OH, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Reddrop IncAtlanta, GA, United StatesManufacturer0000api.fda.gov
Tampon Tribe IncSanta Monica, CA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
The Flex CompanyVenice, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Usa Sun Paper IncMaspeth, NY, United StatesManufacturer0000api.fda.gov

Updated November 2, 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.