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Home›USA›Spectrum Spine, Inc.

Spectrum Spine, Inc.

USA · Jasper
✓ 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
1listed device types
Class I 0Class II 1Class III 0
plus 1 registration records and 9 510(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 States1 registration records, 9 510(k), 0 PMA, 41 excluded
Brazil0 confirmed, 7 excluded
Canada0 confirmed, 8 excluded
Manufacturer names merged into this page: SPECTRUM SPINE INC

Company information

Country
USA
City
Jasper

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

32013 · K130066
12019 · K173518
12021 · K201024
12024 · K240838
22025 · K253377
12026 · K252240

FDA listed device types

Intervertebral Fusion Device With Bone Graft, Cervical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK252240Spectrum Spine Cervical Cage System; Spectrum Spine Lumbar Cage System2026-03-30
USK253377Expandable Titanium PLIF/TLIF System2025-10-24
USK243074Spectrum Spine Lumbar Cage System2025-04-04

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