HomeGermanySTORZ AM MARK GMBH

STORZ AM MARK GMBH

Germany · Emmingen-Liptingen
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Canada, Taiwan, Australia, Israel — 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
66listed device types
Class I 65Class II 1Class III 0
plus 67 registration records and 2 510(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
6valid device licences
Class I 6
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
44active ARTG entries
Class I 40IIa 3IIb 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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 States67 registration records, 2 510(k), 0 PMA, 14 excluded
Saudi Arabia0 confirmed, 2 excluded
Canada1 confirmed, 0 excluded
Manufacturer names merged into this page: STORZ AM MARK GMBH

Company information

Country
Germany
City
Emmingen-Liptingen

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

12005 · K051871
12008 · K080430

FDA listed device types

showing 8 of 66
Curette, Periodontic 1Scissors, Surgical Tissue, Dental 1Clamp 1Forceps, Tooth Extractor, Surgical 1Instrument, Hand, Calculus Removal 1Handle, Scalpel 1Forceps, Articulation Paper 1Accessories, Implant, Dental, Endosseous 1

Registration details (sample)

MarketIdentifierNameClass / date
USK080430STOMA BONE BLOCK SCREW2008-11-21
USK051871STOMA BONE SCREW2005-10-27
CA73301STOMA TITANIUM BONE SCREWSClass III

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