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Data / Medical devices / Unit, Syringe, Air And/Or Water / United States

FDA-registered makers of Unit, Syringe, Air And/Or Water in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Unit, Syringe, Air And/Or Water (product code ECB). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

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Device
Unit, Syringe, Air And/Or Water
Product code
ECB
Country
United States

Makers of Unit, Syringe, Air And/Or Water in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
A-dec, Inc.Newberg, OR, United StatesManufacturer, Repackager or relabeler1November 29, 1993000api.fda.gov
Dentsply LLCYork, PA, United StatesManufacturer, Specification developer1May 3, 1992000api.fda.gov
Accs Products, Inc.Lake Zurich, IL, United StatesManufacturer0000api.fda.gov
Beaverstate Dental, Inc.Newberg, OR, United StatesManufacturer0000api.fda.gov
Busse Hospital DisposablesHauppauge, NY, United StatesManufacturer0000api.fda.gov
Crosstex InternationalRush, NY, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
DCI International, LLCNewberg, OR, United StatesManufacturer0000api.fda.gov
Dentsply Sirona Orthodontics Inc.Sarasota, FL, United StatesContract manufacturer0000api.fda.gov
Hager Worldwide, Inc.Hickory, NC, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Integra LifeSciences Production CorporationMansfield, MA, United StatesSpecification developer0000api.fda.gov
Kerr CorporationPomona, CA, United StatesReprocessor0000api.fda.gov
Nucare LLCMontclair, CA, United StatesSpecification developer0000api.fda.gov
Palmero Healthcare LLCNorthbrook, IL, United StatesSpecification developer0000api.fda.gov
Parts Warehouse IncLynden, WA, United StatesManufacturer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Tidi Products, LLCNeenah, WI, United StatesManufacturer0000api.fda.gov
Young Dental Manufacturing Co 1, LLC.Earth City, MO, United StatesContract manufacturer0000api.fda.gov
Young Innovations Inc.Algonquin, IL, United StatesSpecification developer0000api.fda.gov
Young Microbrush LLCGrafton, WI, 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.