Skip to the page
Get started free

Data / Medical devices / Needle, Conduction, Anesthetic (W/Wo Introducer) / United States

FDA-registered makers of Needle, Conduction, Anesthetic (W/Wo Introducer) in the United States: 28 establishments

28 establishments in the United States are registered with the FDA to make Needle, Conduction, Anesthetic (W/Wo Introducer) (product code BSP). 22 have a 510(k) clearance or PMA approval on file and 6 have a recall event. FDA data exported November 3, 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.

Get makers of this device in the United StatesWatch these makers
Device
Needle, Conduction, Anesthetic (W/Wo Introducer)
Product code
BSP
Country
United States

Makers of Needle, Conduction, Anesthetic (W/Wo Introducer) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
B. Braun Us Device Manufacturing LLCAllentown, PA, United StatesContract manufacturer, Contract sterilizer, Repackager or relabeler9June 27, 2014020api.fda.gov
Epimed International, Inc.Johnstown, NY, United StatesManufacturer, Repackager or relabeler6February 7, 2008010api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer5June 12, 2018000api.fda.gov
BD Puerto Rico LLCJuncos, PR, United StatesManufacturer4July 1, 2022000api.fda.gov
Becton DickinsonFranklin Lakes, NJ, United StatesSpecification developer4July 1, 2022010api.fda.gov
Spectra Medical Devices, LLCWilmington, MA, United StatesManufacturer, Specification developer4September 8, 2017000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer4August 21, 2019010api.fda.gov
Avanos Medical, Inc.Alpharetta, GA, United StatesComplaint file establishment, Specification developer3September 25, 2008000api.fda.gov
B. Braun Medical Inc.Bethlehem, PA, United StatesSpecification developer3June 27, 2014000api.fda.gov
Busse Hospital DisposablesHauppauge, NY, United StatesManufacturer, Repackager or relabeler3January 5, 2018000api.fda.gov
International Medical Development, Inc.Huntsville, UT, United StatesRepackager or relabeler, Specification developer3February 2, 2018000api.fda.gov
Argon Medical Devices, Inc.Wheeling, IL, United StatesContract manufacturer, Manufacturer2January 8, 1999000api.fda.gov
Arrow International LLC (subsidiary of Teleflex Incorporated)Morrisville, NC, United StatesSpecification developer2August 21, 2019011api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer2June 7, 2018000api.fda.gov
Advance Medical Designs, Inc.Marietta, GA, United StatesManufacturer, Repackager or relabeler1October 19, 1989000api.fda.gov
Aerin Medical Inc.Mountain View, CA, United StatesComplaint file establishment, Specification developer1March 21, 2024000api.fda.gov
Argon Medical Devices Inc.Athens, TX, United StatesContract manufacturer, Manufacturer, Repackager or relabeler1January 8, 1999000api.fda.gov
Arrow International, LLC (subsidiary of Teleflex Incorporated)Wyomissing, PA, United StatesSpecification developer1April 25, 2018010api.fda.gov
Bard Access Systems, Inc.Salt Lake City, UT, United StatesComplaint file establishment, Manufacturer for export1June 27, 2017000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer1June 17, 2011000api.fda.gov
Solo-DexWolf Creek, MT, United StatesManufacturer1January 22, 2016000api.fda.gov
Stryker InstrumentsPortage, MI, United StatesSpecification developer1April 5, 2017000api.fda.gov
Eagle Labs, LLCSaint Paul, MN, United StatesContract manufacturer0000api.fda.gov
G3 MedicalSwannanoa, NC, United StatesContract manufacturer0000api.fda.gov
Hart Enterprises, Inc.Sparta, MI, United StatesContract manufacturer0000api.fda.gov
Ispg, Inc.Lakewood Ranch, FL, United StatesContract manufacturer0000api.fda.gov
Pro-Tech Design & MFG., Inc.Santa Fe Springs, CA, United StatesContract manufacturer0000api.fda.gov
Ranfac Corp.Avon, MA, United StatesContract manufacturer0000api.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.