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Data / Medical devices / Cannula, Injection / United States

FDA-registered makers of Cannula, Injection in the United States: 25 establishments

25 establishments in the United States are registered with the FDA to make Cannula, Injection (product code FGY). 0 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.

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Get makers of this device in the United StatesWatch these makers
Device
Cannula, Injection
Product code
FGY
Country
United States

Makers of Cannula, Injection in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ameri Surgical Instruments Inc.Cincinnati, OH, United StatesSpecification developer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
BD Puerto Rico LLCJuncos, PR, United StatesManufacturer0000api.fda.gov
Becton DickinsonFranklin Lakes, NJ, United StatesSpecification developer0010api.fda.gov
Becton Dickinson And CompanyColumbus, NE, United StatesManufacturer0000api.fda.gov
Becton, Dickinson & Co.Broken Bow, NE, United StatesManufacturer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer0000api.fda.gov
Bausch & Lomb IncorporatedManchester, MO, United StatesManufacturer0000api.fda.gov
Becton, DIckinson and CompanyCanaan, CT, United StatesManufacturer0000api.fda.gov
Cannuflow, Inc.Scotts Valley, CA, United StatesSpecification developer0000api.fda.gov
Currier Mos Plastics LLCSan Jose, CA, United StatesContract manufacturer0000api.fda.gov
Custom Assemblies, Inc.Pine Level, NC, United StatesManufacturer0000api.fda.gov
Conmed CorporationWestborough, MA, United StatesSpecification developer0000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Fetzer Surgical, LLCScottsdale, AZ, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Hobbs Medical, Inc.Stafford Springs, CT, United StatesManufacturer0010api.fda.gov
Ispg, Inc.Lakewood Ranch, FL, United StatesContract manufacturer0000api.fda.gov
Izi Medical Products LLCOwings Mills, MD, United StatesManufacturer0000api.fda.gov
Integra LifeSciences Production CorporationMansfield, MA, United StatesSpecification developer0000api.fda.gov
Kerylos CorporationReno, NV, United StatesSpecification developer0000api.fda.gov
Quality Tech Services, LLCBloomington, MN, United StatesContract manufacturer0000api.fda.gov
Ranfac Corp.Avon, MA, United StatesManufacturer0000api.fda.gov
Signa Medical, Inc.Long Beach, NY, United StatesReprocessor0000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0000api.fda.gov

Updated November 3, 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.