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Home›South Africa›Ortho-Design (Pty), Ltd.

Ortho-Design (Pty), Ltd.

South Africa · Hazelwood
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Israel — 2 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
12listed device types
Class I 5Class II 7Class III 0
plus 17 registration records and 2 510(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
1registrations
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 States17 registration records, 2 510(k), 0 PMA, 110 excluded
Brazil0 confirmed, 36 excluded
Saudi Arabia0 confirmed, 12 excluded
Canada0 confirmed, 13 excluded
Manufacturer names merged into this page: OPTIMIZED ORTHO PTY LTD · ORTHO-DESIGN

Company information

Country
South Africa
City
Hazelwood

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

12021 · K212381
12024 · K242296

FDA listed device types

showing 8 of 12
Acetabular Cup Orientation System 1System, Image Processing, Radiological 1Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented 1Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented 1Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate 1Orthopaedic Surgical Planning And Instrument Guides 1Fastener, Fixation, Nondegradable, Soft Tissue 1Bit, Drill 1

Registration details (sample)

MarketIdentifierNameClass / date
USK242296VersaTap™ Suture Anchor (ADP050); VersaPEEK™ Suture Anchor (APP002); MicroTi™ Suture Anchor (ATP003-M); VersaLat™ Ti Suture Anchor (ADP021-TI); VersaLat™ Suture Anchor (ADP021-PK)2024-08-29
USK212381VersaTap, VersaLat, DueLock, VersaTi, MiniTi2021-12-06

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