12 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Bausch + Lomb Boston Scleral Lens Case
FDA 510(k)
FDA Class 2
·Ophthalmic
Sklar®
FDA UDI
SKLAR CORPORATION·10649111069642·COLLER FCP CVD 6 1/4"
ATRAMAT
FDA UDI
Internacional Farmacéutica, S.A. de C.V.·07500142063756·ATRAMAT SILK SURGICAL SUTURE BLACK USP 3-0 EP 2...
DISCOVERY 3T 16 CH BODY ARRAY COIL (ANTERIOR); DISCOVERY 3T 16 CH BODY ARRAY COIL (POSTERIOR); DISCOVERY 3T 32 CH BODY A
FDA 510(k)
FDA Class 2
·Radiology
DENTAL DIGITAL X-RAY IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Dental
WAVEWRITER ALPHA? 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 2, 2026
DISCOVERY RF180
FDA Adverse Event
Injury
·GENERAL MEDICAL MERATE S.P.A.·Product code JAA·August 2, 2023
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·July 23, 2011
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·June 17, 2013
BONE PIN, 4MM X 140MM
FDA Adverse Event
Injury
·MAKO SURGICAL CORP.·Product code JDW·September 19, 2008
PEDICLE SCREW 03.50.054 PEDICLE SCREW 8X40MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·June 16, 2023
Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve D-F, Model A-TCSE-DF, Sterile.
FDA Enforcement
Class II
·Ongoing·Abbott·April 27, 2022