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ORTHOCOR MEDICAL INC.

USA · Minneapolis

✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 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

8listed device types

Class I 6Class II 2Class III 0

plus 8 registration records and 3 510(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

1 including historic records

TWTaiwanTFDA

0valid device licences

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 States8 registration records, 3 510(k), 0 PMA

Manufacturer names merged into this page: ORTHOCOR MEDICAL INC.

FDA 510(k) clearances by year

22009 · K092044

12013 · K121702

FDA listed device types

Orthosis, Limb Brace 1Joint, Knee, External Brace 1Orthosis, Lumbar 1Orthosis, Truncal/Orthosis, Limb 1Pack, Hot Or Cold, Disposable 1Orthosis, Lumbo-Sacral 1Pad, Heating, Powered 1Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K121702	ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE	2013-05-06
US	K092044	ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE	2009-12-18
US	K091996	ORTHOCOR KNEE SYSTEM BASIC	2009-12-15

ORTHOCOR MEDICAL INC.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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