HomeUSAMidwest Dental Products Corp.

Midwest Dental Products Corp.

USA · Des Plaines
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 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 17Class II 3Class III 0
plus 19 registration records and 5 510(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
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 States19 registration records, 5 510(k), 0 PMA, 26 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: MIDWEST DENTAL
Same-named companies — This database also contains companies with near-identical names: MIDWEST DENTAL. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

Country
USA
City
Des Plaines

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

31996 · K962877
11997 · K964755
11998 · K973800

FDA listed device types

showing 8 of 20
Toothbrush, Powered 1Spring, Orthodontic 1Unit, Syringe, Air And/Or Water 1Absorber, Saliva, Paper 1Instruments, Dental Hand 1Syringe, Periodontic, Endodontic, Irrigating 1Dispenser, Liquid Medication 1Adaptor, Hygiene 1

Registration details (sample)

MarketIdentifierNameClass / date
USK97380023:1 REDUCTION ANGLE1998-03-11
USK964755MICROJET CAVITY PREPARATION SYSTEM1997-09-11
USK962877MIDWEST 300 SE1996-10-18

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