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Home›USA›TOBY ORTHOPEDICS INC.

TOBY ORTHOPEDICS INC.

USA
✓ 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
11listed device types
Class I 9Class II 2Class III 0
plus 11 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class II 1
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
1 including historic records
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 States11 registration records, 2 510(k), 0 PMA
Brazil1 confirmed, 0 excluded
Manufacturer names merged into this page: TOBY ORTHOPAEDICS · TOBY ORTHOPAEDICS, LLC · TOBY ORTHOPEDICS INC.
Same-named companies — This database also contains companies with near-identical names: Toby Orthopaedics, LLC. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

Country
USA

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

12008 · K081608
12013 · K131834

FDA listed device types

showing 8 of 11
Passer 1Screwdriver 1Gauge, Depth 1Bit, Drill 1Retractor 1Tray, Surgical 1Tray, Surgical, Instrument 1Retainer, Surgical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK131834WOLF LONG BONE PLATE SYSTEM2013-11-04
USK081608PROXIMAL HUMERUS SCAFFOLD FIXATION SYSTEM (PHSFS)2008-12-19
BR81208020001Flexor Tendon Sheath Retractor and Suture Retriever/Sheath Dilator KitClass II

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