70 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Surgical Face Mask
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112724·BARRON VACUUM PUNCH 6.75MM
OsteoMed
FDA UDI
OSTEOMED LLC·00845694043199·2.7mm Metatarsal Wedge Plate Module
ANSPACH ANGLED MICRONOSE ATTACHMENT
FDA 510(k)
FDA Class 2
·Neurology
CHILLBUSTER
FDA 510(k)
FDA Class 2
·Cardiovascular
SYRINGE 50ML LL TIP 1ML
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·May 6, 2024
MAGELLAN
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code FMI·March 6, 2026
BD 50ML LUER-LOK SYRINGE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY·Product code FMF·November 12, 2024
ETHICON 3-0 VICRYL RAPIDE 36 IN. ON A CT-1
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAM·April 16, 2025
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 18, 2024
GMK
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·September 17, 2025
M.U.S.T. PEDICLE SCREWS SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025
M.U.S.T. RODS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KWP·April 20, 2026
IFUSE TORQ IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·January 16, 2025
INTERSTIM
FDA Adverse Event
Injury
·MPROC, JUNCOS·Product code EZW·October 17, 2008
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·April 30, 2025
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 27, 2025
GMK REVISION TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·February 27, 2025