10,000 results · 511ms · Sources: EU EUDAMED, US FDA

HOOK PUNCH FORCEPS FOR ARTHROSCOPY

FDA 510(k)
FDA Class 2 ·Orthopedic

MUSE Endostapler

FDA UDI
MEDIGUS LTD·07290014036062·The MUSE System consists of a single patient us...

SerosaFuse® Implantable Fastener Kit

FDA UDI
ENDOGASTRIC SOLUTIONS, INC.·00810275014011·Single kit consists of 1 each R2007 EsophyX Z+ ...

MUSE Staple Cartridge

FDA UDI
MEDIGUS LTD·07290014036079·Each box contains 30 sterile single use cartrid...

7.5mm Cartridge

FDA UDI
ENDOGASTRIC SOLUTIONS, INC.·00810275013021·Cartridge, 20 Fasteners, 0.010" Slot, 7.5mm Web

EsophyX Z+

FDA UDI
ENDOGASTRIC SOLUTIONS, INC.·00810275011089·EsophyX Z+ Fastener Delivery Device with Serosa...

6.5mm & 7.5mm Cartridge

FDA UDI
ENDOGASTRIC SOLUTIONS, INC.·00810275013038·Cartridge, 40 Implantable Fasteners, 6.5mm & 7....

EsophyX Z

FDA UDI
ENDOGASTRIC SOLUTIONS, INC.·00810275011072·EsophyX Z Fastener Delivery Device with SerosaF...

SerosaFuse® 7.5mm Implantable Fastener Cartridges

FDA UDI
ENDOGASTRIC SOLUTIONS, INC.·00810275013052·2 Cartridges, 40 Implantable Fasteners, 7.5mm ...

6.5mm Cartridge

FDA UDI
ENDOGASTRIC SOLUTIONS, INC.·00810275013014·Cartridge, 20 Fasteners, 0.010" Slot, 6.5mm Web

MUSE Console

FDA UDI
MEDIGUS LTD·07290014036529·The Medigus Ultrasonic Surgical Endostapler (MU...

EsophyX2 HD

FDA UDI
ENDOGASTRIC SOLUTIONS, INC.·00810275011065·EsophyX®2 HD Device with SerosaFuse Fasteners a...

Filler, Bone Void, Synthetic Peptide

FDA Pre-Market Approval
FDA Class 3 ·I-FACTOR PEPTIDE ENHANCED BONE GRAFT

Filler, Bone Void, Synthetic Peptide

FDA Pre-Market Approval
FDA Class 3 ·AUGMENT BONE GRAFT

t:slim X2

FDA registration
ZOLLNER ELECTRONICS COSTA RICA LIMITADA·1 product·🇨🇷 Costa Rica

Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant

FDA Pre-Market Approval
FDA Class 3 ·CARTIVA SYNTHETIC CARTILAGE IMPLANT DEVICE

Mr-Guided Focused Ultrasound System

FDA Pre-Market Approval
FDA Class 3 ·EXABLATE NEURO THALAMOTOMY

Neuromodulator For Obesity

FDA Pre-Market Approval
FDA Class 3 ·MAESTRO RECHARGEABLE SYSTEM

Heart-Valve, Non-Allograft Tissue

FDA Pre-Market Approval
FDA Class 3 ·Edwards Pericardial Aortic Bioprosthesis

ZELLESR-20

FDA registration
STERILE SAFEQUIP & CHEMICALS LLP·1 product·🇮🇳 India