15 results · 21ms · Sources: EU EUDAMED, US FDA

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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