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PROFESSIONAL PRODUCTS, INC.

USA · Defuniak Spgs

✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Canada, Australia — 3 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

44listed device types

Class I 42Class II 1Class III 0unclassified 1

plus 44 registration records and 19 510(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

2active device licences

Class II 2

9 including historic records

TWTaiwanTFDA

0valid device licences

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

1active ARTG entries

Class I 1

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 States44 registration records, 19 510(k), 0 PMA, 44 excluded

Brazil0 confirmed, 2 excluded

Saudi Arabia0 confirmed, 6 excluded

Canada2 confirmed, 9 excluded

Manufacturer names merged into this page: PROFESSIONAL PRODUCTS, INC. · PROTECH PROFESSIONAL PRODUCTS, INC. · VALUEMED PROFESSIONAL PRODUCTS LTD.

FDA 510(k) clearances by year

11978

11979

11981

21982

11983

21984

21986

11989

11992

21993

31994

11995

12015

FDA listed device types

showing 8 of 44

Orthosis, Lumbar 1Belt, Pelvic, Traction 1Joint, Hip, External Limb Component 1Splint, Hand, And Components 1Orthosis, Moldable, Supportive, Skin Protective 1Orthosis, Foot Drop 1Component, Traction, Non-Invasive 1Orthosis, Limb Brace 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K151646	ProTech Plus	2015-10-21
US	K954295	MARLENE STOCKINGS & TIGHTS	1995-11-08
US	K926280	STANDARD NEBULIZER HEATER	1994-03-22
CA	95860	VALUEMED PROFESSIONAL VINYL MEDICAL EXAMINATION GLOVES	Class II
CA	95862	VALUEMED PROFESSIONAL BLEND MEDICAL EXAMINATION GLOVES	Class II

PROFESSIONAL PRODUCTS, 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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