103 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla
FDA Pre-Market Approval
FDA Class 2
·CILCO ND:YAG LASER
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·CILCO ND:YAG LASER
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
FDA Pre-Market Approval
FDA Class 3
·CILCO ND:YAG LASER
NA
FDA UDI
Richard Wolf GmbH·04055207043608·TEM OBTURATOR Ø 36MM WL 255MM WL 255mm, reusable
Two Striper
FDA UDI
ABRASIVE TECHNOLOGY, INC.·B868C8400471·Abrasive Point
LIFEPAK 7D
FDA 510(k)
FDA Class 2
·Cardiovascular
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·COAPTITE
COAPTITE INJECTABLE IMPLANT
FDA Adverse Event
Other
·MERZ AESTHETICS, INC (FORMERLY BIOFORM MEDICAL, INC.)·Product code LNM·October 29, 2010
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS INC·Product code LNM·November 4, 2011
COAPTITE INJECTABLE IMPLANT
FDA Adverse Event
Other
·MERZ AESTHETICS, INC (FORMALLY BIOFORM MEDICAL, INC)·Product code LNM·October 29, 2010
COAPTITE INJECTABLE IMPLANT
FDA Adverse Event
Other
·MERZ AESTHETICS, INC. (FORMERLY BIOFORM MEDICAL, INC.)·Product code LNM·October 29, 2010
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS, INC·Product code LNM·November 4, 2011
COAPTITE
FDA Adverse Event
Other
·MERZ AESTHETICS INC·Product code LNM·November 4, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2014
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 20, 2012