HomeUSAM.C. JOHNSON COMPANY INC.

M.C. JOHNSON COMPANY INC.

USA · Fort Myers
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Canada, Australia, Israel — 5 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 6Class II 0Class III 0
plus 5 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
3registered devices
Class I 3
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
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
2active ARTG entries
Class I 2
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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 States5 registration records, 3 510(k), 0 PMA, 65 excluded
Brazil3 confirmed, 11 excluded
Saudi Arabia0 confirmed, 7 excluded
Canada6 confirmed, 9 excluded
Manufacturer names merged into this page: M. C. JOHNSON CO., INC. · M.C. JOHNSON COMPANY INC. · M.C. Johnson CO.

Company information

Country
USA
City
Fort Myers

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

11983 · K832702
11988 · K872525
11995 · K953375

FDA listed device types

Device, Incontinence, Urosheath Type, Non-Sterile 1Holder, Ureteral Catheter 1Polymer Patient Examination Glove 1Medical Glove, Specialty 1Tape And Bandage, Adhesive 1Bedding, Disposable, Medical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK953375NG SECURE1995-09-08
USK872525A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH1988-02-22
USK832702POCKET AID1983-11-17
BR80207930001WOUND SECURE ADESIVO FILME TRANSPARENTEClass I
BR80207930002WOUND SECURE - ALMOFADAS PARA ABSORÇÃO DE EXSUDATOClass I
BR80207930004CATH SEGURE FIXADOR ADESIVOClass I
CA77706NON-ADHESIVE FOAM DRESSING W/BARRIERClass II
CA77707TRANSPARENT FILM DRESSINGClass II
CA77708HYDROCOLLOID DRESSINGClass II

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