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Marketing Development Intl.

USA · Mchenry

✓ 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

27listed device types

Class I 8Class II 16Class III 1unclassified 2

plus 55 registration records and 10 510(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

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 States55 registration records, 10 510(k), 0 PMA, 118 excluded

Brazil0 confirmed, 5 excluded

Saudi Arabia0 confirmed, 3 excluded

Canada0 confirmed, 10 excluded

Manufacturer names merged into this page: AG MARKETING & DEVELOPMENT GROUP INC DBA AGMD GROUP

Same-named companies — This database also contains companies with near-identical names: AG MARKETING & DEVELOPMENT GROUP INC DBA AGMD GROUP. Company name alone cannot separate their registrations, so the figures below may include either.

FDA 510(k) clearances by year

11976

11981

11988 · K881419

31989 · K895957

31990 · K897181

11997 · K953902

FDA listed device types

showing 8 of 27

Gown, Surgical 1Biopsy Needle 1Instrument, Biopsy 1Plate, Fixation, Bone 1Syringe, Piston 1Gown, Isolation, Surgical 1Warmer, Blood, Non-Electromagnetic Radiation 1Screw, Fixation, Bone 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K953902	GIOTTO HIGH TECH (H.T.) MAMMOGRAPHIC SYSTEM	1997-03-19
US	K897181	L.T.C. PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE	1990-03-27
US	K896621	L.T.C. REPLACEMENT GASTROSTOMY TUBE	1990-03-13

Marketing Development Intl.

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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