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Data / Medical devices / Cleaner, Ultrasonic, Medical Instrument / United States

FDA-registered makers of Cleaner, Ultrasonic, Medical Instrument in the United States: 36 establishments

36 establishments in the United States are registered with the FDA to make Cleaner, Ultrasonic, Medical Instrument (product code FLG). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Cleaner, Ultrasonic, Medical Instrument
Product code
FLG
Country
United States

Makers of Cleaner, Ultrasonic, Medical Instrument in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Advanced Sterilization ProductsIrvine, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Alconox, LLCWhite Plains, NY, United StatesSpecification developer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Align Technology, Inc.San Jose, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
BrandmaxJasper, GA, United StatesSpecification developer0000api.fda.gov
Central Solutions, Inc.Kansas City, KS, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Cetylite Industries, Inc.Pennsauken, NJ, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Chemclean CorporationJamaica, NY, United StatesManufacturer0000api.fda.gov
Chemlink Laboratories, LLC.Kennesaw, GA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Coltene/Whaledent Inc.Cuyahoga Falls, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Crest Ultrasonics Corp.Ewing, NJ, United StatesManufacturer0000api.fda.gov
Dentsply LLCMilford, DE, United StatesContract manufacturer0000api.fda.gov
Dentsply LLCYork, PA, United StatesSpecification developer0000api.fda.gov
Diversified Chemical Products, IncWilmington, DE, United StatesContract manufacturer0000api.fda.gov
Fabrication Ent., Inc.Elmsford, NY, United StatesManufacturer0000api.fda.gov
GC America Inc.Alsip, IL, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Intercon Chemical Co.St. Louis, MO, United StatesComplaint file establishment, Contract manufacturer0000api.fda.gov
Isonic Inc.Chicago, IL, United StatesRemanufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
KP Dental LLCWilmington, DE, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Keystone IndustriesMyerstown, PA, United StatesSpecification developer0000api.fda.gov
Keystone Industries - GibbstownGibbstown, NJ, United StatesContract manufacturer0000api.fda.gov
L&R MFG. Co., IncKearny, NJ, United StatesManufacturer0000api.fda.gov
L&R MFG. Co., Inc.Kearny, NJ, United StatesManufacturer0000api.fda.gov
MicroCare MedicalCommerce City, CO, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Onlycare IncDenver, CO, United StatesManufacturer0000api.fda.gov
Premier Dental Products Co.Plymouth Meeting, PA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Pascal International, Inc.Bellevue, WA, United StatesManufacturer0000api.fda.gov
Royal Chemical CompanyMacedonia, OH, United StatesContract manufacturer0000api.fda.gov
Sonic Systems, Inc.Ivyland, PA, United StatesManufacturer0000api.fda.gov
Steris CorporationBreckenridge Hills, MO, United StatesManufacturer for export, Repackager or relabeler0000api.fda.gov
Steris CorporationSaint Louis, MO, United StatesComplaint file establishment, Manufacturer, Manufacturer for export0000api.fda.gov
TBJ IncorporatedChambersburg, PA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
The Ruhof CorporationMineola, NY, United StatesManufacturer0000api.fda.gov
United BiotechDeer Park, NY, United StatesSpecification developer0000api.fda.gov
Vintage Chemical Inc.Fort Wayne, IN, United StatesManufacturer0000api.fda.gov
Young Dental Manufacturing Co 1, LLC.Earth City, MO, United StatesSpecification developer0010api.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.