HomeUSATrilliant Surgical, Ltd.

Trilliant Surgical, Ltd.

USA · Houston
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 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
41listed device types
Class I 23Class II 17Class III 1
plus 61 registration records and 18 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
3registered devices
Class I 3
6 including historic records
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
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 States61 registration records, 18 510(k), 0 PMA
Brazil3 confirmed, 0 excluded
Canada1 confirmed, 0 excluded
Manufacturer names merged into this page: Trilliant Surgical LLC · TRILLIANT SURGICAL LTD. · TRILLIANT SURGICAL · TRILLIANT SURGICAL LTD

Company information

Country
USA
City
Houston

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

12007
12008
32011
32012
22013
22016
32017
12018
12019
12022

FDA listed device types

showing 8 of 41
Template 1Elevator 1Forceps 1Clamp 1Impactor 1Punch, Surgical 1Guide, Surgical, Instrument 1Screwdriver 1

Registration details (sample)

MarketIdentifierNameClass / date
USK212378Arsenal Ankle Plating System2022-02-23
USK191009Arsenal Plating System2019-08-12
USK181898Two-Step Implant System2018-10-26
BR10446510004INSTRUMENTAL PARA IMPLANTES SUBTALARESClass I
BR10446510005INSTRUMENTAIS TWO STEPClass I
BR10446510006Instrumentais para Sistema MIBClass I
CA92485REAMERClass II

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