HomeGermanyINNOVATION MEDITECH GMBH

INNOVATION MEDITECH GMBH

Germany · Unna
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 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
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
7listed device types
Class I 6Class II 1Class III 0
plus 7 registration records and 1 510(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
1active device licences
Class III 1
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
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 States7 registration records, 1 510(k), 0 PMA, 100 excluded
Brazil0 confirmed, 26 excluded
Saudi Arabia0 confirmed, 4 excluded
Canada1 confirmed, 17 excluded
Manufacturer names merged into this page: INNOVATION MEDITECH GMBH

Company information

Country
Germany
City
Unna

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

12013 · K123761

FDA listed device types

Plate, Base, Shellac 1Aligner, Bracket, Orthodontic 1Kit, Earmold, Impression 1Hearing Aid, Air-Conduction, Prescription 1Accessories, Implant, Dental, Endosseous 1Material, Impression Tray, Resin 1Resin, Denture, Relining, Repairing, Rebasing 1

Registration details (sample)

MarketIdentifierNameClass / date
USK123761VITA ENAMIC STAINS2013-03-01
CA91205VITA ENAMIC STAINClass III

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