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Data / Medical devices / Saliva, Artificial / United States

FDA-registered makers of Saliva, Artificial in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Saliva, Artificial (product code LFD). 15 have 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
Saliva, Artificial
Product code
LFD
Country
United States

Makers of Saliva, Artificial in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Haleon US HOLDINGS LLCWarren, NJ, United StatesSpecification developer3January 4, 2013000api.fda.gov
Elevate Oral Care, LLCWest Palm Beach, FL, United StatesComplaint file establishment, Manufacturer, Specification developer2February 27, 2026000api.fda.gov
Laclede, Inc.Rancho Dominguez, CA, United StatesManufacturer2April 19, 2024000api.fda.gov
Procter & Gamble Co., Regulatory AffairsMason, OH, United StatesSpecification developer2April 5, 2021000api.fda.gov
Century Pharmaceuticals, Inc.Indianapolis, IN, United StatesComplaint file establishment, Manufacturer1February 10, 1981000api.fda.gov
Church & Dwight Co., Inc.Princeton, NJ, United StatesComplaint file establishment, Specification developer1March 16, 2018000api.fda.gov
Forward Science Technologies LLCHouston, TX, United StatesManufacturer1December 23, 2015000api.fda.gov
GC America Inc.Alsip, IL, United StatesManufacturer1January 27, 2011000api.fda.gov
Gurunanda LLCBuena Park, CA, United StatesManufacturer, Repackager or relabeler1August 22, 2023000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesManufacturer1March 19, 2018000api.fda.gov
K PharmaceuticalsPhoenix, AZ, United StatesManufacturer1October 21, 2005000api.fda.gov
OraLabs, Inc.Parker, CO, United StatesManufacturer1November 21, 2019000api.fda.gov
Rowpar Pharmaceuticals Inc.Bridgewater, NJ, United StatesComplaint file establishment, Specification developer1May 19, 2025000api.fda.gov
Triumph Pharmaceuticals IncSaint Louis, MO, United StatesSpecification developer1February 15, 2019000api.fda.gov
You First Services, Inc.Buffalo, NY, United StatesManufacturer1May 10, 2017000api.fda.gov
Applied Laboratories, Inc.Columbus, IN, United StatesContract manufacturer0000api.fda.gov
Continental Manufacturing ChemistHuxley, IA, United StatesContract manufacturer0000api.fda.gov
Dental Technologies, Inc.Lincolnwood, IL, United StatesContract manufacturer0000api.fda.gov
Nice-Pak Products, LLCSmyrna, TN, United StatesContract manufacturer0000api.fda.gov
Strukmyer MedicalMesquite, TX, United StatesContract manufacturer0000api.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.