CARESCAPE D19KT VER01

FDA registration

GE Medical Systems Information Technologies - Critikon de Mexico S. de R.L. de C.V.·33 products·🇲🇽 Mexico

CARESCAPE D19KT VER01

FDA registration

GE HEALTHCARE FINLAND OY·33 products·🇫🇮 Finland

Carescape B850

FDA 510(k)

FDA Class 2 ·Cardiovascular

Bernafon

FDA UDI

Bernafon AG·05711584086100·ZR1 B 105, 2.4G NFM DPB MAC/MSIL ZERENA 1

Edge™ Diamond PMI012-3M Pear Minimally Invasive

FDA UDI

CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002738·Diamond dental bur, reusable

SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPL

FDA registration

Synthes (USA) Products LLC·1 product·🇺🇸 United States

Intermedic

FDA registration

INTERMEDIC ARFRAN, S.A.·1 product·🇪🇸 Spain

DEKA RESEARCH & DEVELOPMENT CORP.

FDA registration

DEKA RESEARCH & DEVELOPMENT CORP.·1 product·🇺🇸 United States

Unity Subcutaneous Infusion System For Remodulin

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

Aloe Glide Lubricant

FDA registration

PURE SOURCE, LLC·1 product·🇺🇸 United States

EverLift Submucosal Lifting Agent

FDA registration

GI SUPPLY·1 product·🇺🇸 United States

SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

MODIFIED INTERMEDIC DIODE LASER 980NM SYSTEM (MULTIDIODE SST 200)

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

FDA classification

FDA Class 2 ·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

Powered Laser Surgical Instrument

FDA classification

FDA Class 2 ·Powered Laser Surgical Instrument