HomeFranceMicro-Mega SA

Micro-Mega SA

France · Besançon
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Saudi Arabia, Canada — 4 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
7listed device types
Class I 6Class II 1Class III 0
plus 7 registration records and 13 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
15registered devices
Class I 12Class II 3
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
1registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
24active device licences
Class II 23Class III 1
32 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
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 States7 registration records, 13 510(k), 0 PMA, 16 excluded
Brazil15 confirmed, 3 excluded
Saudi Arabia1 confirmed, 5 excluded
Canada24 confirmed, 0 excluded
Manufacturer names merged into this page: Micro-Mega SA · MICRO-MEGA SA · MICRO MEGA SA · MICRO MEGA · MICRO-MEGA S.A

Company information

Country
France

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

11994
21995
21996
41997
12004
12009
12011
12014

FDA listed device types

Resin, Root Canal Filling 1Handpiece, Direct Drive, Ac-Powered 1Preparer, Root Canal Endodontic 1Reamer, Pulp Canal, Endodontic 1File, Pulp Canal, Endodontic 1Broach, Endodontic 1Epilator, High Frequency, Needle-Type 1

Registration details (sample)

MarketIdentifierNameClass / date
USK123276MM-SEAL2014-03-10
USK103123APEX POINTER+; MEASRUING CABLE, HOOK, LIP CLIP, TOUCH PROBE (ACCESSORIES)2011-03-10
USK081268SONIC AIR MM1500 + (MID), MODEL 504000142009-08-10
BR10068870158MicroMega R-EndoClass I
BR10068870159Revo-S+Class I
BR10068870150MICROMEGA ONE GClass I
SAME0000000318SFDAA00016Nerve Broaches
CA3162MOTEUR A AIR MM 324Class II
CA10745CONTREANGLE IOTEClass II
CA68450INSTRUMENTS VIBRANTS POUR MECASONICClass II

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