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Clinical Technologies, Inc.

USA · Barstow

✓ 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

7listed device types

Class I 5Class II 2Class III 0

plus 7 registration records and 27 510(k), 2 PMA

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

11active device licences

Class III 11

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 States7 registration records, 27 510(k), 2 PMA, 103 excluded

Brazil0 confirmed, 21 excluded

Saudi Arabia0 confirmed, 1 excluded

Canada11 confirmed, 17 excluded

Manufacturer names merged into this page: CLINICAL POLYMER TECHNOLOGIES LTD · PENTRON CLINICAL TECHNOLOGIES, LLC

FDA 510(k) clearances by year

11982

11983

11984

31985

21986

11987

21988

11994

12001

12002

22003

22005

22006

42007

22008

12009

FDA listed device types

Template 1Tube, Laryngectomy 1Bag, Intestine 1Protector, Ostomy 1Orthopedic Manual Surgical Instrument 1Prosthesis, Finger, Constrained, Polymer 1Modular Electromechanical Surgical System 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K091512	BUILD-IT LIGHT CURE	2009-10-30
US	K081887	LUTE-IT II VENEER CEMENT, MODEL NO6	2008-08-29
US	K072064	GRAVILAX TRACTION SYSTEM	2008-04-21
CA	65519	BOND-IT SYSTEM	Class III
CA	65530	EPIPHANY ENDODONTIC OBTURATION SYSTEM	Class III
CA	65607	SIMILE COMPOSITE	Class III

Clinical Technologies, 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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