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Abanza Tecnomed, S.L.

MUTILVA Navarra, ES

ABANZA TECNOMED, S.L. appears in FDA device records in MUTILVA Navarra, ES. FDA records list 4 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
4
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 4 510(k) clearances for Abanza Tecnomed, S.L. between 2022 and 2026. The busiest year on record is 2025, with 2. The most recent is 2026, with 1.

Clearances by year, as a table
510(k) clearance decisions for Abanza Tecnomed, S.L., by decision year
YearClearances
20221
20252
20261
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K253618QuadLock™ Fixation SystemMBISubstantially Equivalent
K250238WasherCap™ Fixation SystemMBISubstantially Equivalent
K243712WasherCap™ Mini Fixation System (Model 45)MBISubstantially Equivalent
K212197WasherCap Fixation SystemMBISubstantially Equivalent

Registered establishments

FDA registered establishments for Abanza Tecnomed, S.L., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30256084393025608439ABANZA TECNOMED, S.L.Calle Nueva 29, MUTILVA Navarra 31192 ES2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain