HomeUSAHelix Medical, Inc.

Helix Medical, Inc.

USA · Carpinteria
✓ 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
18510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 18 510(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
1active device licences
Class II 1
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIa 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 States0 registration records, 18 510(k), 0 PMA, 4 excluded
Canada1 confirmed, 1 excluded
Manufacturer names merged into this page: HELIX MEDICAL, LLC

Company information

Country
USA
City
Carpinteria

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

11989
31990
11991
21992
21993
31994
11999
12002
12008
12010
22013

Registration details (sample)

MarketIdentifierNameClass / date
USK130736BLOM-SINGER ADJUSTABLE BI-FIANGED FISTULA PROSTHESIS2013-12-17
USK131745BLOM-SINGER SEPTAL PERFORATION PROSTHESIS2013-09-17
USK093258BLOM-SINGER INDWELLING TEP OCCLUDER2010-03-03
CA66125SILICONE TUBINGClass II

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