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Frontier Devices, Inc.

1 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
FRONTIER DEVICES CRANIOMAXILLOFACIAL, CRANIO CLOSURE, ORTHOGNATHIC, MANDIBLE RECONSTRUCTION AND MESH SYSTEMS (K091812)Frontier Devices, Inc.2010-05-07

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Every clearance here is in the API, with alerts when new ones post.