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Technical Medical Products, Inc.

USA · Phoenix
✓ 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
12listed device types
Class I 5Class II 7Class III 0
plus 15 registration records and 17 510(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 States15 registration records, 17 510(k), 0 PMA, 62 excluded
Brazil0 confirmed, 9 excluded
Saudi Arabia0 confirmed, 6 excluded
Canada0 confirmed, 3 excluded
Manufacturer names merged into this page: TECHNICAL PRODUCTS, INC. · MEDICAL TECHNICAL PRODUCTS, INC
Same-named companies — This database also contains companies with near-identical names: MEDICAL TECHNICAL PRODUCTS, INC. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

Country
USA
City
Phoenix

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

21987
11988
21990
21991
31994
11995
51997
12002

FDA listed device types

showing 8 of 12
Instrument, Ent Manual Surgical 1Catheter, Multiple Lumen 1Apparatus, Suction, Single Patient Use, Portable, Nonpowered 1Catheter, Irrigation 1Connector, Catheter 1Catheter, Malecot 1Unit, Phacofragmentation 1Elastomer, Silicone Block 1

Registration details (sample)

MarketIdentifierNameClass / date
USK013321SILICONE TRACHEAL T-TUBES2002-06-04
USK970163ALPHA MX (20)/ULTRA PC (30)1997-12-10
USK973385OVAL SHAPES1997-12-05

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