HomeUSAPMT CORPORATION

PMT CORPORATION

USA · Chanhassen
✓ Record-verifiedregistrations found in 8 markets

This company has registrations in United States, Brazil, Canada, Taiwan, Singapore, South Korea, Australia, Israel — 8 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
20listed device types
Class I 8Class II 11Class III 0unclassified 1
plus 29 registration records and 26 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class I 1
4 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
11 including historic records
TWTaiwanTFDA
2valid device licences
Class I 2
SGSingaporeHSA SMDR
5device registrations
CLASS C 1CLASS D 4
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
7active ARTG entries
Class I 3IIa 1IIb 2Class Is (sterile) 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
4registrations
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 States29 registration records, 26 510(k), 0 PMA
Brazil1 confirmed, 0 excluded
Manufacturer names merged into this page: PMT CORP. · PMT CORPORATION · PMT CORPORATION

Company information

Country
USA
City
Chanhassen

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

21983
21984
51988
11989
11990
11991
11993
31994
31997
12004
12005
22009
12012
12016
12020

FDA listed device types

showing 8 of 20
Probe, Radiofrequency Lesion 1Catheter And Tip, Suction 1Cable, Electrode 1Electrode, Cortical 1Marker, Colon 1Stent, Vaginal 1Drape, Surgical, Antimicrobial 1Neurological Stereotaxic Instrument 1

Registration details (sample)

MarketIdentifierNameClass / date
USK202542Allura Vaginal Stent2020-09-30
USK151790PMT Platinum Depthalon Depth Electrode2016-07-14
USK122376PMT TRUSCAN SURFACE ELECTRODE2012-12-19
BR80202250024INSTRUMENTAL PARA ELETRODO PMTClass I

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