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KENT LABORATORIES, INC.

USA · Bellingham

✓ 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

59listed device types

Class I 13Class II 46Class III 0

plus 71 registration records and 40 510(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

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 States71 registration records, 40 510(k), 0 PMA, 15 excluded

Brazil0 confirmed, 1 excluded

Saudi Arabia0 confirmed, 2 excluded

Canada0 confirmed, 1 excluded

Manufacturer names merged into this page: KENT LABORATORIES, INC.

FDA 510(k) clearances by year

71977

151979

11981

21982

61983

51985

41995

FDA listed device types

showing 8 of 59

Antithrombin Iii Quantitation 1Igd, Rhodamine, Antigen, Antiserum, Control 1Fibrinogen And Split Products, Antigen, Antiserum, Control 1Kappa, Fitc, Antigen, Antiserum, Control 1Complement C1q, Antigen, Antiserum, Control 1Igd, Antigen, Antiserum, Control 1Iga, Antigen, Antiserum, Control 1Alpha-2-Macroglobulin, Fitc, Antigen, Antiserum, Control 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K951966	HUMAN PREALBUMIN RADIAL IMMUNODIFFUSION KIT	1995-06-01
US	K951967	HUMAN C1 INACTIVATOR OR C-1 ESTERASE INHIBITOR RADIAL IMMUNODIFFUSION KIT	1995-05-30
US	K951968	HUMAN C1Q RADIAL IMMUNODIFFUSION KIT	1995-05-30

KENT LABORATORIES, 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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