40 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LaserShot M, NaviLase
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260391·
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463141·
Bernafon
FDA UDI
Bernafon AG·05711584086827·ZR3, KIT 312 NFM 85 R BE ZERENA 3
OsteoMed
FDA UDI
OSTEOMED LLC·00845694009577·2.0mm x 8mm Cannulated Lag Screw
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101070·WALTON CONJUNCTIVA RETRACTOR
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070089·Cannulated 2.0 x 8mm Lag Screw Sterile Qty 5
GLIDESHEATH
FDA 510(k)
FDA Class 2
·Cardiovascular
TOUCHPACS SUITE
FDA 510(k)
FDA Class 2
·Radiology
ILAB POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·March 3, 2025
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 2, 2019
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026
ARTICUL/EZE BALL 32 +9 BL
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD·Product code JDI·October 6, 2008
CONTINUUM TRABECULAR METAL SHELL
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code LZO·June 20, 2013
2.7MM/3.5MM LCP LATERAL DISTALFIBULA PLATE 6H/RIGHT/
FDA Adverse Event
Injury
·SYNTHES ELMIRA·Product code HRS·July 28, 2011
PROLENE HERNIA SYSTEM UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·April 3, 2019
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·December 16, 2019
Radius Capspin is a non-sterile instrument for use with other devices in spinal surgery.
FDA Recall
Terminated
·Stryker Spine·Product code LXH·February 19, 2008
Radius Rod Persuader is a non-sterile instrument for use with other devices in spinal surgery.
FDA Recall
Terminated
·Stryker Spine·Product code LXH·February 19, 2008