HomeGermanyDUFNER INSTRUMENTE GMBH

DUFNER INSTRUMENTE GMBH

Germany · Tuttlingen Baden-Wurttemberg
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Taiwan, Australia, Israel, Russia — 5 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
104listed device types
Class I 99Class II 5Class III 0
plus 102 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
0active device licences
TWTaiwanTFDA
3valid device licences
Class I 3
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
7active ARTG entries
Class I 7
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
3registrations
RURussiaRoszdravnadzor
1active registrations
Class 1 1
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 States102 registration records, 1 510(k), 0 PMA
Manufacturer names merged into this page: DUFNER INSTRUMENTE GMBH

Company information

Country
Germany
City
Tuttlingen Baden-Wurttemberg

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

12001 · K002877

FDA listed device types

showing 8 of 104
Chisel, Surgical, Manual 1Gag, Mouth 1Chisel, Bone, Surgical 1Sound, Urethral, Metal Or Plastic 1Forceps, Disconnect 1Fork, Tuning 1Orthopedic Manual Surgical Instrument 1Knife, Orthopedic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK002877MICTEC ENDOSCOPES AND ACCESSORIES2001-02-05

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