Koya Dayspring

FDA registration

KOYA MEDICAL, INC.·1 product·🇺🇸 United States

Koya Ripple

FDA 510(k)

FDA Class 2 ·Cardiovascular

CoRoent

FDA UDI

Nuvasive, Inc.·00887517568212·CoRoent Ant TLIF PEEK, 9x13x28mm 8°

HHM

FDA UDI

Oticon A/S·05707131341037·G200, BTE 13 2.4G 85 C063 HHM

RESMED CORP

FDA registration

RESMED CORP·1 product·🇺🇸 United States

Hemoconcentrators

FDA registration

Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium

RESMED PTY LTD.

FDA registration

RESMED PTY LTD.·1 product·🇦🇺 Australia

Siemens MC9-4

FDA registration

LBN MEDICAL A/S·2 products·🇩🇰 Denmark

DEKA SYNCHRO FT

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION

FDA 510(k)

FDA Class 2 ·Cardiovascular

Sleeve, Limb, Compressible

FDA classification

FDA Class 2 ·Sleeve, Limb, Compressible

Outpatient Cardiac Telemetry

FDA classification

FDA Class 2 ·Outpatient Cardiac Telemetry

Powered Laser Surgical Instrument

FDA classification

FDA Class 2 ·Powered Laser Surgical Instrument