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

FDA-registered makers of Needle, Conduction, Anesthetic (W/Wo Introducer) in Japan: 7 establishments

7 establishments in Japan are registered with the FDA to make Needle, Conduction, Anesthetic (W/Wo Introducer) (product code BSP). 6 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
Needle, Conduction, Anesthetic (W/Wo Introducer)
Product code
BSP
Country
Japan

Makers of Needle, Conduction, Anesthetic (W/Wo Introducer) in Japan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Unisis CorpKita-Hiroshima-shi Hokkaido, JapanContract manufacturer, Manufacturer5June 12, 2018000api.fda.gov
Hakko Co., Ltd.CHIKUMA-SHI Nagano, JapanManufacturer3April 25, 2007000api.fda.gov
Unisis Corp.Koshigaya-shi Saitama, JapanContract manufacturer, Manufacturer2January 14, 2015000api.fda.gov
DR. Japan Co., Ltd.Gyoda City Saitama, JapanManufacturer1June 2, 2000000api.fda.gov
Ever Corp.Nasuhiobara City, TOCHIGI Tokyo, JapanManufacturer1October 9, 1996000api.fda.gov
Top CorporationADACHI-KU Tokyo, JapanManufacturer1September 19, 1984000api.fda.gov
B. Braun Aesculap Japan Co., Ltd.Tochigi, JapanContract 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.