15 results
·
21ms
·
Sources: EU EUDAMED, US FDA
PTA (PROGRESSIVE TIBIAL ALIGNMENT)
FDA 510(k)
FDA Class 2
·Orthopedic
Mini-Mono®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70604031·Mini-Mono-Brackets Edgew. 'N' .018" 200 Brackets
Orthopedic manual surgical instrument
FDA UDI
BAUI BIOTECH CO. LTD.·04718005152872·Sensor ( Double )
Rumor
FDA UDI
Ortho Organizers, Inc.·00190707003937·Rumor .022 UL2 8T 9A 0O
VANGUARD COMPLETE KNEE CRUCIATE RETAINING POROUS & HA FEMUR LEFT 75MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code MBH·December 16, 2016
PRESTIGE IQ BLOOD GLUCOSE TEST SYSTEM, MODEL 507400, 537600, 550600, 561700, 563700
FDA 510(k)
FDA Class 2
·Clinical Chemistry
MODIFICATION TO EBI XFIX DFS OPTIROM ELBOW FIXATOR
FDA 510(k)
FDA Class 2
·Orthopedic
Tablet Battery Bay
FDA UDI
Orthosoft Inc·00887868523915·
Truliant CC
FDA UDI
Exactech, Inc.·10885862625854·TRULIANT DIST. AUG. BLOCK TRIAL SZ 1-2, 15MM
Optetrak Logic
FDA UDI
Exactech, Inc.·10885862287410·LOGIC DIST. AUG. BLOCK TRIAL SZ 1-2, 15MM
HOURGLASS
FDA Adverse Event
Injury
·MEDTRONIC·Product code MQP·June 16, 2014
SCR SFTSLK 2.0 PKG.8X20 STER
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code HWC·March 18, 2020
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 10, 2013
C-LEG/C-LEG TUBE ADAPTER
FDA Adverse Event
Injury
·OTTO BOCK HEALTHCARE PRODUCTS GMBH·Product code ISW·June 10, 2008
THE UNFOLDER® IMPLANTATION SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYB·April 16, 2011