20 results
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42ms
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Sources: EU EUDAMED, US FDA
Highridge Medical, LLC
FDA registration
Highridge Medical, LLC·3 products·🇺🇸 United States
Olive Branch Distribution Center
FDA registration
Olive Branch Distribution Center·3 products·🇺🇸 United States
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
FDA 510(k)
FDA Class 2
·Orthopedic
Smart-Read EZTest Steam Biological Test Pack with Instant Readout Integrator
FDA registration
Mesa Laboratories Bozeman Manufacturing Facility (Zoot)·1 product·🇺🇸 United States
ARGUS LSM Pro, ARGUS LSM Patient Monitor
FDA registration
GUANGDONG BIOLIGHT MEDITECH CO., LTD·3 products·🇨🇳 China
SteriTec Smart Read Biological Test Pack with Instant Readout Integrator
FDA registration
STERITEC PRODUCTS MFG. CO., INC.·1 product·🇺🇸 United States
BONE REDUCTION CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896050969·BONE REDUCTION CLAMP WITH LONG RATCHET
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR21030401·Compound retraction arch max. .016"x.022" / 30°
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515061927·O.R. Sci, S/B, str, 5 3/4"
Needle aspiration and injection
FDA UDI
KATENA PRODUCTS, INC.·00841668113646·RETROBULBAR NEEDLE 23GA 38MM
GPS¿ Anterior Cervical Plate System
FDA registration
G Surgical LLC·1 product·🇺🇸 United States
NICOLET WIRELESS EEG
FDA registration
Natus Neurology Incorporated·2 products·🇺🇸 United States
ATMOS S 201 Thorax
FDA registration
HA2 MEDIZINTECHNIK GMBH·1 product·🇩🇪 Germany
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR21030400101·Compound retraction arch max. .016"x.022" / 30°
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR21030400051·Compound retraction arch max. .016"x.022" / 30°
INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LIGHT SABER INTRODUCER NEEDLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Thoracolumbosacral Pedicle Screw System
FDA classification
FDA Class 2
·Thoracolumbosacral Pedicle Screw System
Instrument, Manual, Surgical, General Use
FDA classification
FDA Class 1
·Instrument, Manual, Surgical, General Use
Stents, Drains And Dilators For The Biliary Ducts
FDA classification
FDA Class 2
·Stents, Drains And Dilators For The Biliary Ducts