25 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACETAL
FDA 510(k)
FDA Class 1
·Dental
OCTAGON Infinity BL NC Basic screw for CAD/CAM
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM50220321·BL NC Basic screw for CAD/CAM for OCTAGON Infin...
10mm Reamer Bit - Sterile
FDA UDI
XIROS LTD·05060267130860·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694018647·2.0mm x 32mm Lag Screw
SOUTHMEDIC, INC.
FDA registration
SOUTHMEDIC, INC.·27 products·🇨🇦 Canada
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710410220320·Anterior Closing Wedge Osteotomy Guide, 22mm x ...
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710420220320·Anterio Lateral Closing Wedge Osteotomy Guide, ...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694066709·HPS 2.0 x 32mm Lag Screw Sterile Qty 5
C02 LASER MULTIPULSE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FIRST SPEP
FDA 510(k)
FDA Class 2
·Dental
8022032-2018-00000
FDA Adverse Event
Injury
·July 31, 2018
SOUTHMEDIC #11 NON-STERILE DISPOSABLE SCALPEL
FDA Adverse Event
Injury
·SOUTHMEDIC INC.·Product code GES·February 25, 2020
APHIS PLATEAU RADIAL T1
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code JWJ·May 19, 2017
30MM TAP
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·March 30, 2021
PRIMEADVANCED
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LGW·March 26, 2013
GLIDEWIRE GT
FDA Adverse Event
Malfunction
·TERUMO·Product code DQX·March 11, 2011
DTC MARGRON HIP REPLACEMENT SYSTEM
FDA Adverse Event
Injury
·PORTLAND ORTHOPAEDICS LTD.·Product code LPH·April 1, 2008
CARDIAC CATH PACK
FDA Adverse Event
Malfunction
·AVID MEDICAL, INC.·Product code OEZ·March 9, 2026
PFNA-II BLADE L90 TAN
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HSB·September 11, 2023
4.5MM TI MULTILOC SCREW LENGTH 42MM-STERILE
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HSB·June 16, 2023