n/a

FDA UDI

HANS RUDOLPH, INC.·00874750006267·4500C SERIES NON HTD PNT

C+B (laser skin surface care)

FDA registration

Sanmina·1 product·🇺🇸 United States

Solta Medical, Inc.

FDA registration

Solta Medical, Inc.·1 product·🇺🇸 United States

AeroDR P-12

FDA registration

KONICA MINOLTA TECHNOPRODUCTS CO., LTD.·1 product·🇯🇵 Japan

Bausch & Lomb Incorporated

FDA registration

Bausch & Lomb Incorporated·1 product·🇺🇸 United States

AeroDR P-12

FDA registration

KONICA MINOLTA, INC.·1 product·🇯🇵 Japan

AeroDR P-12

FDA registration

KONICA MINOLTA, INC.·1 product·🇯🇵 Japan

RS-4s Stimulator

FDA registration

RS MEDICAL·2 products·🇺🇸 United States

TREPONEMA PALLIDUM TREPONEMAL TEST REAGENTS; QUALITY CONTROL MATERIALS

FDA registration

DIAFARMA ECZA DEPOSU VE MEDIKAL DIS TICARET DIS TIC LTD STI·1 product·🇹🇷 Türkiye

METAVISION CLINICAL INFORMATION SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular

AERODR SYSTEM

FDA 510(k)

FDA Class 2 ·Radiology

Laparoscope, General & Plastic Surgery

FDA classification

FDA Class 2 ·Laparoscope, General & Plastic Surgery

Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

System, X-Ray, Stationary

FDA classification

FDA Class 2 ·System, X-Ray, Stationary