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Data / Medical devices / Syringe, Antistick / United States

FDA-registered makers of Syringe, Antistick in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make Syringe, Antistick (product code MEG). 21 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
Syringe, Antistick
Product code
MEG
Country
United States

Makers of Syringe, Antistick in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Duopross Meditech CorporationFarmingdale, NY, United StatesSpecification developer6April 5, 2005000api.fda.gov
Retractable Technologies, Inc.Little Elm, TX, United StatesComplaint file establishment, Manufacturer4February 12, 1998000api.fda.gov
Sol-Millennium Medical, Inc.Chicago, IL, United StatesComplaint file establishment, Specification developer4August 19, 2016000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesComplaint file establishment, Specification developer3October 18, 2023000api.fda.gov
Ulti Med, Inc.De Smet, SD, United StatesSpecification developer3February 9, 2015000api.fda.gov
Becton DickinsonFranklin Lakes, NJ, United StatesComplaint file establishment, Specification developer2June 13, 2001040api.fda.gov
BiometerPlus USA, Inc.Fremont, CA, United StatesSpecification developer2September 11, 2020000api.fda.gov
Greystone Medical, LLCWaterford, MI, United StatesSpecification developer2July 2, 2021000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer2February 27, 2007000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesComplaint file establishment, Specification developer2March 4, 2022000api.fda.gov
Becton Dickinson And CompanyColumbus, NE, United StatesManufacturer1June 13, 2001000api.fda.gov
Becton, DIckinson and CompanyCanaan, CT, United StatesManufacturer1June 13, 2001000api.fda.gov
Care Living Diagnostics IncSouth Setauket, NY, United StatesComplaint file establishment, Specification developer1March 25, 2016000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer1June 21, 2023000api.fda.gov
Cardinal HealthNorfolk, NE, United StatesManufacturer1June 21, 2023000api.fda.gov
Ecomed Solutions, LLCLindenhurst, IL, United StatesComplaint file establishment, Specification developer1March 21, 2008000api.fda.gov
Exelint International, Co.Redondo Beach, CA, United StatesManufacturer, Specification developer1October 19, 2005000api.fda.gov
Embecta Medical II LLCParsippany, NJ, United StatesComplaint file establishment, Specification developer1October 1, 1999000api.fda.gov
Gamamed Vascular Systems Inc.Loveland, CO, United StatesManufacturer, Repackager or relabeler1March 1, 2022000api.fda.gov
Pegasus ImportsHouston, TX, United StatesSpecification developer1March 25, 2016000api.fda.gov
Vault Paragon Group, Inc.Garden City, ID, United StatesComplaint file establishment, Contract manufacturer, Specification developer1January 25, 2023000api.fda.gov
ICU Medical, Inc.Southington, CT, United StatesManufacturer0000api.fda.gov
Isomedix Operations Inc.Northborough, MA, United StatesManufacturer for export0000api.fda.gov
embecta medical I LLCHoldrege, NE, United StatesContract manufacturer, 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.