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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.
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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. JRNY II CR LKG FEM IMP BUMPER LT 03/04/2024
SMITH & NEPHEW, INC. JRNY II CR LKG FEM IMP BUMPER RT 01/23/2024
ZIMMER BIOMET, INC. MC TIBIAL ARTICULAR SURFACE PROVISIONAL 01/02/2024
ZIMMER BIOMET, INC. TIBIAL ARTICULAR SURFACE PROVISIONAL RIG 08/09/2023
ZIMMER BIOMET, INC. PS TIBIAL ARTICULAR SURFACE PROVISIONAL 07/13/2023
SMITH & NEPHEW, INC. JRNY II CR LKG FEM IMP BUMPER RT 03/16/2023
ZIMMER/BIOMET, INC. ZIMMER BIOMET TRIAL 03/10/2023
SMITH & NEPHEW, INC. JRNY II BCS ART ISRT TRL SZ 7-8 9MM RT 02/15/2023
SMITH & NEPHEW, INC. UNIV ISRT SPACER SZ3-4 13M 07/07/2022
SMITH & NEPHEW, INC. JRN II BCS LCK FEM IMPLANT IMPACT 06/11/2022
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