38 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEALIX ADVANCE KNOTLESS BR Anchor
FDA 510(k)
FDA Class 2
·Orthopedic
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010586·PedFuse, Set Screw, 5-7mm
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481122583·LOCATOR R-Tx Attachment System for 2.2mm Platfo...
CONMED
FDA UDI
Conmed Corporation·30653405010214·CONMED ELECTROSURGICAL ACCESSORY, Loop Excision...
HAEMATOKRIT 200
FDA UDI
Andreas Hettich GmbH·04050674077842·bench-top centrifuge without rotor
EBA 200
FDA UDI
Andreas Hettich GmbH·04050674077804·Tabletop centrifuge
Super Upper Limbs Versalock Plating System
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258665696·VERSALOCK RSL WRIST FUSION PLATE, DORSAL, LEFT
HAEMATOKRIT 200
FDA UDI
Andreas Hettich GmbH·04050674092746·bench-top centrifuge with rotor
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100943·JAFFE LID RETRACTOR SMALL
AAP CANNULATED SCREW AND DARCO HEADED SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
GSP NEONATALGALT KIT, MODEL 3303-001U
FDA 510(k)
FDA Class 2
·Clinical Chemistry
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197537056·Glasser Micro Needleholder
diamon...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197519267·CCR/CLR Caspar Handle for blades,SideLoa
cannul...
UNKNOWN GEL IMPLANTS
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·November 2, 2022
PEDFUSE
FDA Adverse Event
Malfunction
·SPINEFRONTIER, INC·Product code MNI·October 17, 2017
PEDFUSE
FDA Adverse Event
Malfunction
·SPINEFRONTIER, INC·Product code MNH·October 13, 2017
PEDFUSE
FDA Adverse Event
Malfunction
·SPINEFRONTIER, INC·Product code MNH·October 17, 2017
PEDFUSE
FDA Adverse Event
Malfunction
·SPINEFRONTIER, INC·Product code MNH·October 12, 2017
STYLE 110 SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·April 14, 2026
REDUCTION SCREW EXTENDER (STAINLESS STEEL)
FDA Adverse Event
Malfunction
·ALPHATEC SPINE INC·Product code LXH·May 18, 2016