HomeUSAMEDICAL DISPOSABLES CORP

MEDICAL DISPOSABLES CORP

USA · Orlando
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Saudi Arabia — 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
34listed device types
Class I 8Class II 24Class III 0unclassified 2
plus 16 registration records and 6 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
3registered 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 States16 registration records, 6 510(k), 0 PMA, 15 excluded
Saudi Arabia3 confirmed, 1 excluded
Canada0 confirmed, 3 excluded
Manufacturer names merged into this page: MEDICAL DISPOSABLES CORP · ACROSS MEDICAL DISPOSABLES CO., LTD. · HENGXIN (VN) MEDICAL DISPOSABLES CO., LTD. · ACTIV MEDICAL DISPOSABLES

Company information

Country
USA
City
Orlando

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

11976 · K761078
51977 · K771231

FDA listed device types

showing 8 of 34
Electrosurgical, Cutting & Coagulation & Accessories 1Enzyme Immunoassay, Opiates 1Pneumoperitoneum Needle 1Enzyme Immunoassay, Benzodiazepine 1Laparoscope, General & Plastic Surgery 1Test, Benzodiazepine, Over The Counter 1Test, Tricyclic Antidepressants, Over The Counter 1Enzyme Immunoassay, Amphetamine 1

Registration details (sample)

MarketIdentifierNameClass / date
USK771231ARTEOIAL LINE KIT1977-08-16
USK771230PERCUTANEOUS INTRODUCER SHEATH SET1977-08-16
USK770945POUCH, TYVEK-POLYMYLON1977-06-29
SAME0000001195SFDAA00001Finea
SAME0000001195SFDAA00002FINEA SLIP

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