HomeUSAMICROMEDICS, INC.

MICROMEDICS, INC.

USA · St. Paul
✓ Record-verifiedregistrations found in 8 markets

This company has registrations in United States, Brazil, Canada, Taiwan, Singapore, Australia, Hong Kong, 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
6listed device types
Class I 4Class II 2Class III 0
plus 19 registration records and 29 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
9registered devices
Class I 1Class II 8
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
4active device licences
Class II 3Class III 1
10 including historic records
TWTaiwanTFDA
7valid device licences
Class II 7
SGSingaporeHSA SMDR
1device registrations
CLASS B 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
4active ARTG entries
IIa 4
HKHong KongMDACS
1valid listings
Class II 1
ILIsraelAMAR
5registrations
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 States19 registration records, 29 510(k), 0 PMA, 1 excluded
Brazil9 confirmed, 0 excluded
Canada4 confirmed, 0 excluded
Manufacturer names merged into this page: MICROMEDICS, INC.

Company information

Country
USA
City
St. Paul

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

31983
11984
11986
21988
21989
21991
11994
11998
31999
12001
12004
32005
12006
12008
12010
12011
22012
12013
12024

FDA listed device types

Regulator, Pressure, Gas Cylinder 1Syringe, Irrigating (Non Dental) 1Accessories, Catheter 1Cannula, Surgical, General & Plastic Surgery 1Laparoscope, General & Plastic Surgery 1Syringe, Piston 1

Registration details (sample)

MarketIdentifierNameClass / date
USK241739Endoscopic Applicator, 41 cm2024-07-15
USK123847MALLEABLE TIP ENDOSCOPIC APPLICATOR2013-01-08
USK122526360 GAS ASSISTED ENDOSCOPIC APPLICATOR2012-11-16
BR80978569028Aplicadores ArthrexClass II
BR80145240407Aplicador Tisseel DuploSpray Cirurgia Minimamente InvasivaClass II
BR80145240408Aplicador Coseal DuploSpray Cirurgia Minimamente InvasivaClass II
CA23084S & T OSSICULAR REPLACEMENT PROSTHESIS - TITANIUMClass III
CA83887VISCOSPRAY & VISCOGEL DELIVERY APPLICATORSClass II
CA88196APPLICATOR KITSClass II

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