5,696 results
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89ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RootMend MRR
FDA 510(k)
FDA Class 2
·Orthopedic
RootMend™ MRR
FDA UDI
RIVERPOINT MEDICAL, LLC·00840277405593·Titanium Button
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749045512·Ball joint adapter (D8) for MRR-2/MRP-1
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749045604·Ball joint adapter d4 f. MRP-1 right side
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749045581·Ball joint adapter d4 f. MRP-1 left side
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749045529·Ball joint adapter (D4) with distance elevator ...
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749125009·Myocardial stabilizer with ball joint connector...
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749045543·Ball joint adapter (D4) with dista. elevator f....
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749045567·Myocardial stabilizer with ball joint connector...
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749045536·Ball joint adapter (D4) with distance elev. f. ...
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749119879·Myocardial stabilizer with ball joint connector...
RootMend™ MRR (Black)
FDA UDI
RIVERPOINT MEDICAL, LLC·00840277405579·Adjustable Loop
RootMend™ MRR (Blue)
FDA UDI
RIVERPOINT MEDICAL, LLC·00840277405586·Adjustable Loop
RootMend™ MRR Soft Button (Black)
FDA UDI
RIVERPOINT MEDICAL, LLC·00840277405647·Adjustable Loop
RootMend™ MRR Soft Button (Blue)
FDA UDI
RIVERPOINT MEDICAL, LLC·00840277405654·Adjustable Loop
ACUFEX DIRECTOR MRR ANGLED BULLET
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code NBH·August 14, 2024
ACUFEX DIRECTOR MRR ANGLED BULLET
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code NBH·August 31, 2020
ACUFEX DIRECTOR MRR ANGLED BULLET
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code NBH·May 2, 2024
130 DEG AIMING ARM F/TROCHANTERIC FIXATION NAILS
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code JDS·October 26, 2012
TI LCP® VOLAR DISTAL RADIUS PLATE EXTRA-ARTICULAR/LEFT
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·December 18, 2017