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Data / Medical devices / Dissector, Surgical, General & Plastic Surgery / China

FDA-registered makers of Dissector, Surgical, General & Plastic Surgery in China: 13 establishments

13 establishments in China are registered with the FDA to make Dissector, Surgical, General & Plastic Surgery (product code GDI). 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
Dissector, Surgical, General & Plastic Surgery
Product code
GDI
Country
China

Makers of Dissector, Surgical, General & Plastic Surgery in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
B.Braun Medical (Suzhou) Co,.LtdSuzhou Jiangsu, ChinaContract manufacturer0000api.fda.gov
Beijing Bohaikangyuan Medical Devices Co.,ltd.Beijing Economic and Technological Development Area, ChinaManufacturer0000api.fda.gov
Beijing Fule Science & Technology Development Co., Ltd.Beijing, ChinaManufacturer0000api.fda.gov
Beilun Plastech IncNingbo Zhejiang, ChinaContract manufacturer0000api.fda.gov
Bothwin (Beijing) Medical Technology Co., Ltd.Beijng Beijing, ChinaManufacturer0000api.fda.gov
Hangzhou Endo Medical Instrument Co.,ltdhangzhou Zhejiang, ChinaManufacturer0000api.fda.gov
Hangzhou Kangji Medical Instrument Co., Ltd.HANGZHOU Zhejiang, ChinaManufacturer0000api.fda.gov
Jiangsu Guangda Medical Material Group Co., Ltd.Haian Jiangsu, ChinaManufacturer0000api.fda.gov
Shandong Weigao Orthopaedic Device Co.,ltdweihai Shandong, ChinaContract manufacturer0000api.fda.gov
SHANGHAI KiNETIC MEDICAL CO LTDShanghai, ChinaContract manufacturer0000api.fda.gov
Shanghai Lange Medtech Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Shanghai Medical Instruments (group) Ltd. Corp.Shanghai, ChinaManufacturer0000api.fda.gov
Xinhua Surgical Instrument Co. Ltd.ZIBO Shandong, ChinaManufacturer0000api.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.