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Data / Medical devices / Dilator, Nasal / United States

FDA-registered makers of Dilator, Nasal in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Dilator, Nasal (product code LWF). 0 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
Dilator, Nasal
Product code
LWF
Country
United States

Makers of Dilator, Nasal in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Apex Dental Sleep LabLa Mesa, CA, United StatesContract manufacturer0000api.fda.gov
Aso LLCSarasota, FL, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Breathewave Technologies Inc.Edgewater, NJ, United StatesSpecification developer0000api.fda.gov
CranioMandibular Rehab, Inc.Wheat Ridge, CO, United StatesManufacturer0000api.fda.gov
Dream RecoveryDorchester, MA, United StatesSpecification developer0000api.fda.gov
G & G Products, LLCKennebunk, ME, United StatesComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
In'tech IndustriesRamsey, MN, United StatesContract manufacturer0000api.fda.gov
Innomed Healthscience, Inc.Deerfield Bch, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Intake Breathing Technology LLCSanta Barbara, CA, United StatesManufacturer0000api.fda.gov
Kobayashi America Manufacturing, LLCDalton, GA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
KX Medical, Inc.Gallatin, TN, United StatesContract manufacturer0000api.fda.gov
M&M Pure Air Systems LLCLewes, DE, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Medtech Products, Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Neilmed Pharmaceuticals, Inc.Santa Rosa, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Protego LLCMountlake Ter, WA, United StatesSpecification developer0000api.fda.gov
Respire LLCGreenville, DE, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Sanostec CorpBeverly, MA, United StatesSpecification developer0000api.fda.gov
Somnifix International LLCChevy Chase, MD, United StatesSpecification developer0000api.fda.gov
Scapa Tapes North America, LLCKnoxville, TN, United StatesContract manufacturer0000api.fda.gov
Vivos Therapeutics INC.Murray, KY, United StatesSpecification developer0000api.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.