Data / Medical devices / Vietnam / Nam Ha Viet Nam Trading Company Limited
Nam Ha Viet Nam Trading Company Limited: FDA-registered device maker in Hanoi Ha Noi, Vietnam, 38 510(k) clearances
Nam Ha Viet Nam Trading Company Limited is registered with the FDA (registration 3018507299) in Hanoi Ha Noi, Vietnam. It lists 26 device types. The FDA files 38 510(k) clearances under its listings, the newest dated July 25, 2025. Registered through 2026. 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.
- FDA registration number
- 3018507299
- Address
- NO10, LK10-06, Doc Bun 1, La Khe Ward, Ha Dong district, Hanoi Ha Noi, Vietnam, LK10-06
- Owner or operator
- TAS MEDICAL SUPPLY (10027831)
- Roles
- Exporter to the US, Repackager or relabeler
- First device listed
- June 16, 2016
- Registered through
- 2026
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 25, 2025 | K243403 | BD Nexiva Closed IV Catheter System | FOZ | Substantially Equivalent | Becton Dickinson Infusion Therapy Systems, Inc. | accessdata.fda.gov |
| November 27, 2024 | K241353 | PowerLoc Max Power Injectable Infusion Set; SafeStep Huber Needle Set | PTI | Substantially Equivalent | Bard Access Systems, Inc. | accessdata.fda.gov |
| April 6, 2020 | K193217 | SensiCare PI and SensiCare PI Micro Surgical Gloves | KGO | Substantially Equivalent | Medline Industries, Inc. | accessdata.fda.gov |
| November 20, 2018 | K182288 | TPH Spectra ST Flowable Composite Restorative | EBF | Substantially Equivalent | Dentsply Sirona | accessdata.fda.gov |
| July 2, 2018 | K173276 | Medline Sterile Water USP and Medline Sterile 0.9% Normal Saline USP | FRO | Substantially Equivalent | Medline Industries, Inc. | accessdata.fda.gov |
| February 5, 2015 | K143209 | SonicFill 2 | EBF | Substantially Equivalent | Sybron Dental Specialties | accessdata.fda.gov |
| February 21, 2014 | K133948 | BARD(R) MONOPTY(R) DISPOSABLE CORE BIOPSY INSTRUMENT, BARD(R) MAX-CORE(R) DISPOSABLE CORE INSTRUMENT | KNW | Substantially Equivalent | Bard Peripheral Vascular, Inc. | accessdata.fda.gov |
| August 22, 2013 | K131432 | CLEARFIL SE BOND 2 KIT; CLEARFIL SE BOND 2 VALUE PACK; CLEARFIL SE BOND 2 TRIAL PACK; CLEARFIL SE BOND 2 BOND; CLEARFIL | KLE | Substantially Equivalent | Kuraray Noritake Dental, Inc. | accessdata.fda.gov |
| January 20, 2011 | K103351 | DMC COMPOSITE 2 | EBF | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| April 8, 2010 | K094007 | UNICEM | EMA | Substantially Equivalent | 3M Espe AG Dental Products | accessdata.fda.gov |
| December 17, 2008 | K083610 | FILTEK SUPREME ULTRA UNIVERSAL RESTORATIVE | EBF | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| July 21, 2008 | K081229 | SAF-T CLOSED BLOOD COLLECTION SYSTEM WITH SAF-HOLDER DEVICE, WITH 21G, 23G, 25G SAF-T WING | JKA | Substantially Equivalent | Smiths Medical Asd, Inc. | accessdata.fda.gov |
| February 26, 2008 | K080253 | KIMBERLY-CLARK INTRODUCER KITS | KGC | Unknown | Kimberly-Clark Corp. | accessdata.fda.gov |
| August 15, 2007 | K071742 | BEAUTIFIL II | EBF | Substantially Equivalent | Shofu Dental Corp. | accessdata.fda.gov |
| August 2, 2007 | K071785 | HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE, HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE WITH SYRINGE | FMI | Substantially Equivalent | Smiths Medical Asd, Inc. | accessdata.fda.gov |
| December 10, 2004 | K043114 | KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE | KNT | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| July 2, 2003 | K031444 | OPTIBOND FL | KLE | Substantially Equivalent | Kerr Dental Materials Center | accessdata.fda.gov |
| August 10, 2000 | K001655 | PERMLASTIC 2 | ELW | Substantially Equivalent | Kerr Corp. | accessdata.fda.gov |
| July 17, 2000 | K001730 | GC FUJICEM | EMA | Substantially Equivalent | GC America, Inc. | accessdata.fda.gov |
| January 11, 2000 | K993973 | FUJI II LC CAPSULE | EBF | Substantially Equivalent | GC America, Inc. | accessdata.fda.gov |
| October 8, 1999 | K992326 | 3M CLINPRO SEALANT | EBC | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| September 8, 1999 | K992897 | IMPREGUM PENTA | ELW | Substantially Equivalent | Espe Dental AG | accessdata.fda.gov |
| November 27, 1996 | K963735 | COJET SYSTEM | EBF | Substantially Equivalent | Espe GmbH & Co. Kg. | accessdata.fda.gov |
| August 12, 1996 | K962785 | 3M DENT SYSTEM | KLE | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| July 18, 1996 | K962065 | 3M VITREBOND LIGHT CURE GLASS IONOMER/BASE | EMA | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| May 16, 1996 | K960954 | KETAC-MOLAR APLICAP | EMA | Substantially Equivalent | Espe GmbH & Co. Kg. | accessdata.fda.gov |
| October 7, 1995 | K951254 | SAFETYGLIDE NEEDLE | FMI | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| April 25, 1995 | K951123 | CAVICIDE SURFACE DISINFECTANT/DECONTAMINANT CLEANER | LRJ | Substantially Equivalent | Micro-Aseptic Products, Inc. | accessdata.fda.gov |
| April 6, 1995 | K950787 | WELCH ALLYN OTOSCOPE | ERA | Substantially Equivalent | Welch Allyn, Inc. | accessdata.fda.gov |
| November 17, 1994 | K943642 | HERCULITE XR & XRV | EBF | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| April 29, 1994 | K924830 | LUXATEMP AUTOMIX | EBG | Substantially Equivalent | Dmg Chemisch Pharmazeutische Fabrik GmbH | accessdata.fda.gov |
| March 20, 1992 | K920424 | SCOTCHBOND BRAND MULTI-PURPOSE ADHESIVE SYSTEM | KLE | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| April 13, 1990 | K900447 | DUODERM* ADHESIVE COMPRESSION BANDAGE | KGX | Substantially Equivalent | Convatec, A Division of E.R. Squibb & Sons | accessdata.fda.gov |
| September 18, 1989 | K894219 | TEMP BOND NE | EMA | Substantially Equivalent | Kerr Corporation (Danbury) | accessdata.fda.gov |
| October 31, 1988 | K881422 | COE PAK AUTO MIX, REGULAR OR HARD SET | EMA | Substantially Equivalent | Coe Laboratories, Inc. | accessdata.fda.gov |
| March 25, 1985 | K844846 | ESPE KETAC-CEM RADIOPAQUE | EMA | Substantially Equivalent | Espe GmbH (Us) | accessdata.fda.gov |
| June 2, 1981 | K811291 | TEGADERM TRANSPARENT DRESSING | KGX | Substantially Equivalent | 3M Company | accessdata.fda.gov |
| June 2, 1981 | K811160 | SUR-FIT IRRIGATION SLEEVE | EXD | Substantially Equivalent | E. R. Squibb & Sons, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Cement, Dental
- All makers of Agent, Tooth Bonding, Resin
- All makers of Material, Tooth Shade, Resin
- All makers of Bag, Drainage, With Adhesive, Ostomy
- All makers of Disinfectant, Medical Devices
- All makers of Tube, Gastro-Enterostomy
Updated July 25, 2025. 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.