AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

AESCULAP PEEK XP SPINAL IMPLANT SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Oticon

FDA UDI

Oticon A/S·05707131257505·H15, BTE 13 WL 85 STG

Ophthalmic Spatula

FDA UDI

KATENA PRODUCTS, INC.·00841668102961·PISACANO NUCLEUS ROTATOR VERTICAL

WELCH MEDICAL LLC

FDA registration

WELCH MEDICAL LLC·1 product·🇺🇸 United States

COMPASS HEALTH BRANDS (CORPORATE OFFICE)

FDA registration

COMPASS HEALTH BRANDS (CORPORATE OFFICE)·1 product·🇺🇸 United States

EMG Suction Unit

FDA registration

Mediair Inc.·1 product·🇨🇳 China

Suction unit AME-EPS

FDA registration

AMELIFE LLC·1 product·🇺🇸 United States

CAPSULE ENDSCOPE SYSTEM

FDA registration

JAPAN GAS COMPANY LIMITED·1 product·🇯🇵 Japan

MAJ-2027

FDA registration

SHIRAKAWA OLYMPUS CO., LTD.·1 product·🇯🇵 Japan

EMG Suction Unit

FDA registration

EMG TECHNOLOGY CO., LTD.·1 product·🇹🇼 Taiwan

MAJ-2027

FDA registration

OLYMPUS MEDICAL SYSTEMS CORP.·1 product·🇯🇵 Japan

RBCX Exchange Set

FDA registration

Terumo BCT, Inc..·1 product·🇺🇸 United States

cavity Varnish

FDA registration

Summit Packaging Solutions LLC·1 product·🇺🇸 United States

cavity Varnish

FDA registration

Summit Packaging Solutions LLC·1 product·🇺🇸 United States

EMG SUCTION UNIT

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

AMBU PEDIATRIC MULTI-FUNCTION DEFIBRILLATION ELECTRODE

FDA 510(k)

FDA Class 3 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Apparatus, Suction, Ward Use, Portable, Ac-Powered

FDA classification

FDA Class 2 ·Apparatus, Suction, Ward Use, Portable, Ac-Powered

Automated External Defibrillators (Non-Wearable)

FDA classification

FDA Class 3 ·Automated External Defibrillators (Non-Wearable)