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Home›USA›Medi-Dyne Instruments, Inc.

Medi-Dyne Instruments, Inc.

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
8listed device types
Class I 8Class II 0Class III 0
plus 8 registration records and 5 510(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 States8 registration records, 5 510(k), 0 PMA, 10 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: MEDI-DYNE HEALTHCARE PRODUCTS, INC.
Same-named companies — This database also contains companies with near-identical names: MEDI-DYNE HEALTHCARE PRODUCTS, INC.. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

Country
USA
City
Mchenry

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

11979 · K792379
21993 · K931833
11997 · K970401
12000 · K000825

FDA listed device types

Joint, Knee, External Brace 1Patient Personal Hygiene Kit 1Orthosis, Truncal/Orthosis, Limb 1Massager, Therapeutic, Manual 1Insoles, Medical 1Pack, Hot Or Cold, Reusable 1Apparatus, Traction, Non-Powered 1Dressing, Wound, Hydrogel Without Drug And/Or Biologic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK0008254F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER2000-09-21
USK970401MEDI-DYNE GUIDING CATHETER1997-08-01
USK931833MODIFIED LUER1993-09-28

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