13 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Straumann® BLC and TLC Implants - Line extension
FDA 510(k)
FDA Class 2
·Dental
M.U.S.T. PEDICLE SCREWS SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025
Leaseir MHR Xcell
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORM
FDA 510(k)
FDA Class 2
·Dental
M.U.S.T. PEDICLE SCREW SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·January 13, 2026
M.U.S.T. PEDICLE SCREWS SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025
INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·August 28, 2020
INTIMA-II 22GAX1.00IN PRN SLM NPVC
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·August 19, 2019
DURACON UNIVERSAL B/P NON-BEADED
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·August 29, 2011
EXTRACTOR RX RETRIEVAL BALLOON
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code FGE·November 4, 2008
SERVO-S
FDA Adverse Event
Other
·MAQUET CRITICAL CARE AB·Product code CBK·July 15, 2013
M.U.S.T. SACRAL ILIAC SCREW AND PELVIC TRAUMA SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code OUR·October 16, 2024
K-Wire Trochar Tip, Model Number 212000008 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma.
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·July 10, 2019