HomeTaiwanINNOVATIVE MEDICAL MANUFACTURING CO.

INNOVATIVE MEDICAL MANUFACTURING CO.

Taiwan · Zhunan Township Miaoli County
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Australia — 2 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
17listed device types
Class I 7Class II 10Class III 0
plus 27 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
Class I 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States27 registration records, 3 510(k), 0 PMA, 109 excluded
Brazil0 confirmed, 10 excluded
Saudi Arabia0 confirmed, 4 excluded
Canada0 confirmed, 15 excluded
Manufacturer names merged into this page: INNOVATIVE MEDICAL MANUFACTURING CO.

Company information

Country
Taiwan
City
Zhunan Township Miaoli County

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12007 · K070801
12009 · K090727
12013 · K131661

FDA listed device types

showing 8 of 17
Introducer, Syringe Needle 1Syringe, Piston 1Set, I.V. Fluid Transfer 1Catheter, Coude 1Catheter, Straight 1Set, Administration, Intravascular 1Needle, Hypodermic, Single Lumen 1Container, Empty, For Collection & Processing Of Blood & Blood Components 1

Registration details (sample)

MarketIdentifierNameClass / date
USK131661INFUSION SYRINGE SET2013-11-05
USK090727IMM DENTAL IRRIGATION TUBING SET2009-08-13
USK070801IMM HYPODERMIC NEEDLE SET2007-05-24

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