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Data / Medical devices / Gauze / Sponge,Nonresorbable For External Use / Vietnam

FDA-registered makers of Gauze / Sponge,Nonresorbable For External Use in Vietnam: 10 establishments

10 establishments in Vietnam are registered with the FDA to make Gauze / Sponge,Nonresorbable For External Use (product code NAB). 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
Gauze / Sponge,Nonresorbable For External Use
Product code
NAB
Country
Vietnam

Makers of Gauze / Sponge,Nonresorbable For External Use in Vietnam

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Allmed Medical Textile Co.,ltd (viet Nam)Tan Lan Commune Tay Ninh, VietnamContract manufacturer0000api.fda.gov
An Lanh Investment And Trading Company LimitedThanh Nam Ward Ninh Binh, VietnamManufacturer0000api.fda.gov
Bong Bach Tuyet Joint Stock CompanyHo Chi Minh, VietnamManufacturer0000api.fda.gov
Global Resources (vietnam) Group Limited CompanyHai Phong City, VietnamContract manufacturer0000api.fda.gov
Hameco Hy Co., LtdHung Yen Province, VietnamContract manufacturer, Manufacturer0000api.fda.gov
Quang Nam Medical Devices Factory Branch Of Danameco Medical Joint Stock CorporationDien Ban Bac Ward Da Nang, VietnamManufacturer0000api.fda.gov
Stevimed Medical Joint Stock CompanyCan Giuoc Commune Tay Ninh, VietnamManufacturer0000api.fda.gov
Sanqi (Vietnam) New Material Co., LtdTan Phuoc 3 Commune Dong Thap, VietnamManufacturer0000api.fda.gov
United Technology Vietnam Company LimitedQuang Ha Commune Quang Ninh, VietnamContract manufacturer0000api.fda.gov
Vien Phat Import Export Service Trading Joint Stock CompanyBen Thanh Ward Ho Chi Minh, VietnamManufacturer0000api.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.