HomeUSAULTIMATE WIREFORMS, INC.

ULTIMATE WIREFORMS, INC.

USA · Bristol
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Canada, Taiwan, South Korea, Australia, Israel — 6 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
4listed device types
Class I 4Class II 0Class III 0
plus 4 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
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
5active device licences
Class II 5
TWTaiwanTFDA
2valid device licences
Class I 2
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
2GMP quality-system certificates
Import 2
AUAustraliaTGA ARTG
4active ARTG entries
IIa 4
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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 States4 registration records, 6 510(k), 0 PMA
Canada5 confirmed, 0 excluded
Manufacturer names merged into this page: ULTIMATE WIREFORMS, INC. · ULTIMATE WIREFORMS INC

Company information

Country
USA
City
Bristol

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

31992 · K923836
21993 · K924805
11996 · K960799

FDA listed device types

Spring, Orthodontic 1Clamp, Wire, Orthodontic 1Wire, Orthodontic 1Tube, Orthodontic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK960799ORTHO-ICE1996-05-09
USK924805ORTHODONTIC ARCH WIRE1993-03-31
USK923837DIMPLED MULTI MODULUS ARCH WIRE1993-03-31
CA98916STAINLESS STEEL ORTHODONTIC SPRINGSClass II
CA98917NICKEL TITANIUM SPRINGSClass II
CA98918NICKEL TITANIUM ORTHODONTIC WIREClass II

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