78 results · 29ms · Sources: EU EUDAMED, US FDA

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Implant, Intragastric For Morbid Obesity

FDA Pre-Market Approval
FDA Class 3 ·Spatz3 Adjustable Balloon System

Implant, Intragastric For Morbid Obesity

FDA Pre-Market Approval
FDA Class 3 ·Spatz3 Adjustable Balloon System

Implant, Intragastric For Morbid Obesity

FDA Pre-Market Approval
FDA Class 3 ·Spatz3 Adjustable Balloon System

Implant, Intragastric For Morbid Obesity

FDA Pre-Market Approval
FDA Class 3 ·Spatz3 Adjustable Balloon System

Casco

FDA UDI
CASCO MANUFACTURING SOLUTIONS, INC.·00815073028321·SEALED COT MATTRESS

Greenwald Surgical Company, Inc.

FDA UDI
GRACE MANUFACTURING, INC.·10801334007447·Otis bougie-a-boule. stainless steel

PIRANHA

FDA UDI
SPINAL ELEMENTS·00840916112165·1-L CERV PLATE-12mm

iTotal PS

FDA UDI
Conformis, Inc.·M572RPS0101900121·ITOTAL PS - IPOLY - 19MM INSERT – LEFT or right...

devemed

FDA UDI
devemed GmbH·04061644021277·Filling instrument, spatulate # 3 2.0 / 2.0 mm ...

Reicodent

FDA UDI
devemed GmbH·04061644050734·Filling instrument, spatulate # 3 2.0 / 2.0 mm ...

iTotal PS

FDA UDI
Conformis, Inc.·M572RPS0201900121·ITOTAL PS IPOLY XE - 19MM INSERT - LEFT or righ...

SilverGlide

FDA UDI
STRYKER CORPORATION·04546540695871·ProSeries Non-stick Bipolar Electrosurgical For...

SILVERGLIDE

FDA UDI
STRYKER CORPORATION·04546540532084·Non-Stick Bipolar Electrosurgical Standard Forc...

SILVERGLIDE

FDA UDI
STRYKER CORPORATION·04546540532404·Non-Stick Bipolar Electrosurgical Forceps SI Ba...

OMNI-STAT Vascular (Rapid); CELOX Vascular Rapid

FDA 510(k)
FDA Unclassified ·Unknown

Optical Diagnostic Device For Melanoma Detection

FDA Pre-Market Approval
FDA Class 2 ·MELAFIND

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval
FDA Class 3 ·NUVASIVE PCM CERVICAL DISC SYSTEM

Reicodent

FDA UDI
devemed GmbH·04061644034918·Filling instrument, spatulate # 3 2.0 / 2.0 mm ...

TREO ABDOMINAL STENT-GRAFT SYSTEM

FDA Adverse Event
Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·July 12, 2022

TREO ABDOMINAL STENT-GRAFT SYSTEM

FDA Adverse Event
Injury ·BOLTON MEDICAL, INC.·Product code MIH·February 16, 2021