30 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
NA
FDA UDI
Smith & Nephew, Inc.·03596010037824·STAPLE HAMMER
OmniLab Advanced Plus
FDA UDI
Respironics, Inc.·00606959021525·OmniLab Advanced Plus with Heated Humidifier, I...
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390829694·
Stryker
FDA UDI
Provision·00810041060402·
Stryker
FDA UDI
Provision·B504OM41111270900·
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390862615·
NA
FDA UDI
STERILMED, INC.·10888551030465·SAW BLADE SAGITTAL DUAL CUT SYSTEM 4, SYSTEM 20...
NA
FDA UDI
STRYKER CORPORATION·04546540216816·Dual Cut Sagittal Blade
N/A
FDA UDI
STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825013363·Dual Cut Sagittal Saw Blade
PATIENT MONITOR, MODEL PM50
FDA 510(k)
FDA Class 2
·Cardiovascular
PRELUDE III TONGUE SUSPENSION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
TI TITAMAX IMPLANT (4.1)3.75X11
FDA Adverse Event
Injury
·NEODENT - JJGC S.A.·Product code DZE·November 8, 2017
ONE TOUCH PROFILE
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·April 23, 2002
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·October 20, 2023
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·February 23, 2023
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 8, 2025
HXPE LINER ELEVATED II 32
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·May 21, 2024
PROLENE POLYPROPYLENE MESH
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·May 14, 2013
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 23, 2014