IMPLANET

France · Martillac Nouvelle-Aquitaine

✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Singapore, Australia, Hong Kong, 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

14listed device types

Class I 3Class II 11Class III 0

plus 24 registration records and 3 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

5registered devices

Class I 5

7 including historic records

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

1device registrations

CLASS C 1

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

3active ARTG entries

Class I 1IIa 1IIb 1

HKHong KongMDACS

2valid listings

Class III 1Class IV 1

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 States24 registration records, 3 510(k), 0 PMA, 1 excluded

Brazil5 confirmed, 0 excluded

Manufacturer names merged into this page: IMPLANET

FDA 510(k) clearances by year

12024 · K240392

12025 · K252437

12026 · K254017

FDA listed device types

showing 8 of 14

Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis 1Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 1Thoracolumbosacral Pedicle Screw System 1Appliance, Fixation, Spinal Intervertebral Body 1Orthosis, Spinal Pedicle Fixation 1Orthosis, Spondylolisthesis Spinal Fixation 1Intervertebral Fusion Device With Bone Graft, Lumbar 1Cerclage, Fixation 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K254017	SWINGO-3D Lumbar Cage System	2026-02-26
US	K252437	JAZZ Spinal System	2025-08-28
US	K240392	JAZZ Spinal System	2024-05-06
BR	80519830017	Kit Instrumental MADISON	Class I
BR	80519830008	Kit Instrumental JAZZ	Class I
BR	80519830010	Kit Instrumental HAKA	Class I

IMPLANET

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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