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Motiva USA, LLC

New York, NY, US

Motiva USA, LLC appears in FDA device records in New York, NY. FDA records list 2 510(k) clearances between and , 3 PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
2
PMA records
3
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 2 510(k) clearances for Motiva USA, LLC between 2019 and 2023. The busiest year on record is 2019, with 1. The most recent is 2023, with 1.

Clearances by year, as a table
510(k) clearance decisions for Motiva USA, LLC, by decision year
YearClearances
20191
20231
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K211676Motiva Flora SmoothSilk Tissue ExpanderLCJSubstantially Equivalent
K183163Intraoperative, Single-Use, Sterile, Silicone Breast Sizer Motiva Implant MatrixMRDSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

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