HomeUSATOTAL JOINT ORTHOPEDICS, INC.

TOTAL JOINT ORTHOPEDICS, INC.

USA · Salt Lake City
✓ 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
21listed device types
Class I 12Class II 9Class III 0
plus 40 registration records and 31 510(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 States40 registration records, 31 510(k), 0 PMA, 13 excluded
Brazil0 confirmed, 3 excluded
Manufacturer names merged into this page: TOTAL JOINT ORTHOPEDICS, INC.

Company information

Country
USA
City
Salt Lake City

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

12010
12012
52014
52015
32016
22017
22018
32019
12020
22021
22022
22023
12025
12026

FDA listed device types

showing 8 of 21
Screwdriver 1Template 1Reamer 1Wrench 1Bit, Drill 1Broach 1Extractor 1Impactor 1

Registration details (sample)

MarketIdentifierNameClass / date
USK261734Klassic Infection Spacer System2026-07-23
USK243991Klassic Knee System - Revision Tibial Baseplate2025-03-24
USK232414Klassic® Tibial Insert, PS-Post, Klassic All Poly Tibia, PS-Post2023-09-08

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