HomeUSAMICRO MEDICAL DEVICES, INC.

MICRO MEDICAL DEVICES, INC.

USA · Calabasas
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Australia, Israel — 3 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
11listed device types
Class I 8Class II 3Class III 0
plus 10 registration records and 10 510(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
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
Class I 1IIa 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 States10 registration records, 10 510(k), 0 PMA, 118 excluded
Brazil0 confirmed, 28 excluded
Saudi Arabia0 confirmed, 4 excluded
Canada0 confirmed, 10 excluded
Manufacturer names merged into this page: MICRO MEDICAL DEVICES, INC.

Company information

Country
USA
City
Calabasas

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

11988
21994
31995
11997
11999
12001
12006

FDA listed device types

showing 8 of 11
Digital Visual Acuity Test 1Tester, Color Vision 1Pupillograph 1Instrument, Measuring, Stereopsis 1Adaptometer (Biophotometer), Software-Based Data Acquisition And Stimulus Generation 1Perimeter, Automatic, Ac-Powered 1Haploscope 1Topographer, Corneal, Battery Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
USK061283PULMOLIFE2006-12-14
USK003695MICROSCOPE-STAINLESS STEEL/FIBER OPTIC: .5-2.6MM MODEL MMD 4500 SERIES AND 2.7-5.0MM MODEL MMD-4700 SERIES2001-02-14
USK983882MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-14001999-03-15

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