HomeGermanyGEOMED MEDIZIN-TECHNIK GMBH & CO. KG

GEOMED MEDIZIN-TECHNIK GMBH & CO. KG

Germany · Tuttlingen
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Canada, Taiwan, Australia, Israel, Russia — 6 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
47listed device types
Class I 39Class II 8Class III 0
plus 47 registration records and 4 510(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
6active device licences
Class II 6
TWTaiwanTFDA
2valid device licences
Class I 2
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
29active ARTG entries
Class I 26IIa 2Class Im (measuring) 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
4active registrations
Class 1 4
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 States47 registration records, 4 510(k), 0 PMA, 1 excluded
Canada6 confirmed, 0 excluded
Manufacturer names merged into this page: GEOMED MEDIZIN-TECHNIK GMBH & CO. KG

Company information

Country
Germany
City
Tuttlingen

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 · K052745
12010 · K102048
12019 · K183438
12020 · K201279

FDA listed device types

showing 8 of 47
Instrument, Ent Manual Surgical 1Scissors, Orthopedic, Surgical 1Clamp 1Rongeur, Mastoid 1Forceps, Tooth Extractor, Surgical 1Punch, Tonsil 1Clamp, Surgical, General & Plastic Surgery 1Scissors, Ophthalmic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK201279ASSISTO Universal Applicator Clamping Device2020-07-10
USK183438Geomed Vascular Dilators2019-09-03
USK102048ATRAUMATIC VASCULAR CLAMPS2010-11-09
CA72084BIOPSY FORCEPS AND CURETTESClass II
CA72085SUCTION AND ASPIRATING CURETTESClass II
CA72087HEMORRHOIDAL LIGATORClass II

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