40 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ORIA CERVICAL PLATES
FDA 510(k)
FDA Class 2
·Orthopedic
BIOMEDICS UV COLORS (OCUFILCON D) SOFT (HYDROPHILIC) CONTACT LENS
FDA 510(k)
FDA Class 2
·Ophthalmic
FERMIT N PLUS
FDA 510(k)
FDA Class 2
·Dental
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
RINGLOC-X ARCOMXL H/W 50/32MM 23
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·May 10, 2016
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
RINGLOC-X ARCOMXL H/W 54/36MM 24
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 1, 2016
RINGLOC-X ARCOM LINER
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2017
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 26, 2024
RINGLOC-X E1 H/W 60/36MM 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2016
RINGLOC-X E1 H/+3MM 50/36MM 23
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·February 1, 2016
ARCOM XL HI-WALL LINER RINGLOC-X SZ 46MM (RINGLOC SIZE 22)
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 29, 2016
RINGLOC-X E1 H/W 60/36MM 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2016
ARCOM XL HI-WALL LINER RINGLOC-X SZ 54MM (RINGLOC SIZE 24)
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·April 20, 2016