HomeUSAOhio Medical Corporation

Ohio Medical Corporation

USA · Gurnee
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, Singapore, Israel — 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
35listed device types
Class I 11Class II 24Class III 0
plus 54 registration records and 82 510(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
4active device licences
Class II 4
12 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
6device registrations
CLASS B 6
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
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 States54 registration records, 82 510(k), 0 PMA, 9 excluded
Brazil0 confirmed, 1 excluded
Canada4 confirmed, 1 excluded
Manufacturer names merged into this page: Nissha Medical Technologies (Ohio), Inc. · Ohio Medical LLC · OHIO MEDICAL LLC

Company information

Country
USA
City
Gurnee

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

61977
21978
31979
91980
81981
81982
111983
101984
31985
11989
11990
31993
11994
11995
21996
21998
21999
22002
12006
12008

FDA listed device types

showing 8 of 35
Forceps, Biopsy, Non-Electric 1Accessories, Cleaning Brushes, For Endoscope 1Laryngoscope, Rigid 1Flowmeter, Tube, Thorpe, Back-Pressure Compensated 1Forceps, General & Plastic Surgery 1Regulator, Pressure, Gas Cylinder 1Scissors, General, Surgical 1Surgical Instruments, G-U, Manual (And Accessories) 1

Registration details (sample)

MarketIdentifierNameClass / date
USK081185MOBLVAC W.C.2008-05-02
USK062610CARE-E-VAC 32006-09-28
USK021604MAYFIELD RADIOLUCENT SKULL PINS, MODEL 4-0-A-20202002-07-29
CA65307VENTURI/EJECTOR SUCTION MODULEClass II
CA76706AIR-OXYGEN BLENDERClass II
CA88221REUSABLE HUMIDIFIER BOTTLEClass II

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