HomeSpainABANZA TECNOMED, S.L.

ABANZA TECNOMED, S.L.

Spain · Mutilva Navarra
✓ 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
10listed device types
Class I 9Class II 1Class III 0
plus 13 registration records and 4 510(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 States13 registration records, 4 510(k), 0 PMA
Manufacturer names merged into this page: ABANZA TECNOMED, S.L.

Company information

Country
Spain
City
Mutilva Navarra

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

12022 · K212197
22025 · K250238
12026 · K253618

FDA listed device types

showing 8 of 10
Screwdriver 1Positioner, Socket 1Bit, Drill 1Countersink 1Handle, Scalpel 1Awl 1Tray, Surgical, Instrument 1Set, Hollow Mill 1

Registration details (sample)

MarketIdentifierNameClass / date
USK253618QuadLock™ Fixation System2026-01-06
USK250238WasherCap™ Fixation System2025-02-25
USK243712WasherCap™ Mini Fixation System (Model 45)2025-01-30

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