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PROPPER MFG. CO., INC.

USA · Long Island City

✓ 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

9listed device types

Class I 4Class II 5Class III 0

plus 29 registration records and 25 510(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

6active device licences

Class II 5Class III 1

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 States29 registration records, 25 510(k), 0 PMA, 1 excluded

Saudi Arabia0 confirmed, 2 excluded

Canada6 confirmed, 0 excluded

Manufacturer names merged into this page: PROPPER MFG. CO., INC. · PROPPER MFG. CO. INC.

FDA 510(k) clearances by year

31977

11980

11981

21982

21984

11985

11987

31990

21992

11997

21998

11999

12001

12004

12009

12011

12012

FDA listed device types

showing 8 of 9

Reagent, Occult Blood 1Indicator, Physical/Chemical Sterilization Process 1Wrap, Sterilization 1Indicator, Biological Sterilization Process 1Indicator, Sterilization 1Laryngoscope, Rigid 1Hemocytometer 1Blade, Scalpel 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K111453	STEAM DOT BLU PROCESS INDICATOR	2012-04-05
US	K102894	CLASSIX CHEMICAL STERILIZATION INDICATOR	2011-05-25
US	K082620	ONCE-A-DAY VERTOS TEST PACK	2009-07-08
CA	73380	FIBER OPTIC LARYNGOSCOPE BLADE	Class II
CA	82660	PROPPER SERACULT FECAL OCCULT BLOOD TEST	Class III
CA	84578	FLIP-TIP MAC LARYNGOSCOPE BLADE	Class II

PROPPER MFG. CO., 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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