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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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5 records meeting your search criteria returned- Product Code: LXH Patient Problem: Arthralgia Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
ORTHO DEVELOPMENT n/a 05/12/2022
ORTHO DEVELOPMENT N/A 12/03/2020
ORTHO DEVELOPMENT ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 09/28/2020
ORTHO DEVELOPMENT FEMORAL HEAD TRIAL 08/11/2020
ORTHO DEVELOPMENT IMPACTOR 06/05/2020
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