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Data / Medical devices / Adaptor, Holder, Syringe / United States

FDA-registered makers of Adaptor, Holder, Syringe in the United States: 27 establishments

27 establishments in the United States are registered with the FDA to make Adaptor, Holder, Syringe (product code IQG). 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
Adaptor, Holder, Syringe
Product code
IQG
Country
United States

Makers of Adaptor, Holder, Syringe in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Andwin ScientificSimi Valley, CA, United StatesManufacturer0000api.fda.gov
Arthrex, Inc.Naples, FL, United StatesSpecification developer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
AbbVie IncNorth Chicago, IL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
AbbVie US LLCNorth Chicago, IL, United StatesManufacturer0000api.fda.gov
Certa DoseDenver, CO, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Core Products International IncChetek, WI, United StatesManufacturer0000api.fda.gov
Exelint International, Co.Redondo Beach, CA, United StatesManufacturer, Specification developer0000api.fda.gov
EmCyte CorporationFort Myers, FL, United StatesManufacturer0000api.fda.gov
Genia Medical, Inc.Orlando, FL, United StatesManufacturer for export0000api.fda.gov
Hospira, Inc.Mcpherson, KS, United StatesManufacturer0000api.fda.gov
Injecta Medical LLCHialeah, FL, United StatesSpecification developer0000api.fda.gov
Innomed, Inc.Savannah, GA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Instrumental Machine & Development, Inc.Warsaw, IN, United StatesContract manufacturer0000api.fda.gov
Kellida IncAtlanta, GA, United StatesManufacturer0000api.fda.gov
Made, University Of IowaIowa City, IA, United StatesManufacturer0000api.fda.gov
Medela LLCMchenry, IL, United StatesSpecification developer0000api.fda.gov
Plas-Tech Engineering, LLCLake Geneva, WI, United StatesContract manufacturer0000api.fda.gov
Pro-Tech Design & MFG., Inc.Santa Fe Springs, CA, United StatesContract manufacturer0000api.fda.gov
PRO-TECH Design & Mfg, Inc.Santa Fe Springs, CA, United StatesContract manufacturer0000api.fda.gov
Pain Away Solutions LLCMerced, CA, United StatesManufacturer0000api.fda.gov
Rapid Aid Corp.Moberly, MO, United StatesComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
SMC Ltd.Devens, MA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Staley House LLCHelena, AR, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
SpineSmith Holdings, LLCAustin, TX, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
TempramedSammamish, WA, United StatesManufacturer, Specification developer0000api.fda.gov
VGI medical, LLCLargo, FL, United StatesManufacturer0000api.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.