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Kinamed, Incorporated

USA · Camarillo

✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Canada, Taiwan, Australia, Israel — 6 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

13listed device types

Class I 3Class II 10Class III 0

plus 12 registration records and 35 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

4registered devices

Class I 2Class II 2

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

4 including historic records

TWTaiwanTFDA

3valid device licences

Class I 1Class II 2

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

6active ARTG entries

IIa 1IIb 5

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

5registrations

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 States12 registration records, 35 510(k), 0 PMA

Brazil4 confirmed, 1 excluded

Manufacturer names merged into this page: KINAMED, INC. · KINAMED INCORPORATED

FDA 510(k) clearances by year

11988

21989

51990

31991

61992

11994

21995

11997

11998

12000

22001

22002

22003

12004

12005

12007

12011

12013

12018

FDA listed device types

showing 8 of 13

Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component 1Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer 1Screw, Fixation, Intraosseous 1Plate, Fixation, Bone 1Cerclage, Fixation 1Plate, Cranioplasty, Preformed, Alterable 1Fastener, Plate, Cranioplasty 1Screw, Fixation, Bone 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K181749	SuperCable® Iso-Elastic Cerclage System	2018-08-01
US	K122049	NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEM	2013-04-05
US	K102834	ISO-ELASTIC CERCLAGE SYSTEM (1MM AND 2MM CABLE DIAMETER)	2011-01-12
BR	80218280013	CARBOJET REGULADOR DE PRESSÃO DE CO2	Class I
BR	80218280012	SISTEMA DE LAVAGEM COM CO2 CARBOJET	Class II
BR	80218280005	CARBOJET DESCARTAVEL	Class II

Kinamed, Incorporated

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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