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Osartis GmbH

Muenster Hesse, DE

OSARTIS GMBH appears in FDA device records in Muenster Hesse, DE. FDA records list 6 510(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
6
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 6 510(k) clearances for Osartis GmbH between 2019 and 2024. The busiest year on record is 2021, with 3. The most recent is 2024, with 1.

Clearances by year, as a table
510(k) clearance decisions for Osartis GmbH, by decision year
YearClearances
20192
20213
20241
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K240856Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer MoldsMBBSubstantially Equivalent
K202458BonOs Inject, Pedicle screw kits, Cement pusherLODSubstantially Equivalent
K210125BonOs HV Genta, BonOs MV Genta, BonOs LV GentaLODSubstantially Equivalent
K210120BonOs HV, BonOs MV, BonOs LVLODSubstantially Equivalent
K192394Hi-Fatigue Bone CementLODSubstantially Equivalent
K192379Hi-Fatigue G Bone CementLODSubstantially Equivalent

Registered establishments

FDA registered establishments for Osartis GmbH, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
96150143005568854OSARTIS GMBHAuf der Beune 101, Muenster Hesse 64839 DE2026

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