Sterigenics US, LLC

FDA registration

Sterigenics US, LLC·5 products·🇺🇸 United States

FLEX-CELL PRECISION, INC.

FDA registration

FLEX-CELL PRECISION, INC.·5 products·🇺🇸 United States

Hipp Medical AG

FDA registration

Hipp Medical AG·5 products·🇩🇪 Germany

BRANCH MEDICAL GROUP

FDA registration

BRANCH MEDICAL GROUP·5 products·🇺🇸 United States

AMERICAN MANUFACTURING AND ENGINEERING

FDA registration

AMERICAN MANUFACTURING AND ENGINEERING·5 products·🇺🇸 United States

BRANCH MEDICAL GROUP

FDA registration

BRANCH MEDICAL GROUP·5 products·🇺🇸 United States

FIRST ARTICLE INC

FDA registration

FIRST ARTICLE INC·5 products·🇺🇸 United States

ODP - Intervertebral fusion device with bone graft, cervical

FDA registration

B & G MFG. CO.·5 products·🇺🇸 United States

PATRIOT TPS Spacers

FDA registration

GLOBUS MEDICAL, INC.·5 products·🇺🇸 United States

SUSTAIN R TPS Spacers, PATRIOT TPS Spacers, CALIBER TPS Spacer, COALITION TPS Spacers, INDEPENDENCE TPS Spacer, FORTIFY -R TPS Corpectomy Spacer, FORTIFY I-R TPS Corpectomy Spacer, XPand -R TPS Corpectomy Spacer, NIKO TPS Corpectomy Spacer

FDA 510(k)

FDA Class 2 ·Orthopedic

Philips NM3 Respiratory Monitor w/VentAssist

FDA registration

Philips Electronics Ltd·1 product·🇨🇦 Canada

The 4CIS Spinal System and 4CIS Low Back

FDA registration

ALPHANOX CO., LTD.·2 products·🇰🇷 South Korea

The 4cis Spinal System And 4cis Low Back

FDA registration

SOLCO BIOMEDICAL CORP.·2 products·🇺🇸 United States

Philips NM3 Respiratory Monitor w/VentAssist

FDA registration

CEVA LOGISTICS LIMITED·1 product·🇬🇧 United Kingdom

Philips NM3 Respiratory Monitor w/VentAssist

FDA registration

CEVA LOGISTICS NETHERLANDS BV (Venray)·1 product·🇳🇱 Netherlands

Philips NM3 Respiratory Monitor w/VentAssist

FDA registration

RESPIRONICS NOVAMETRIX, LLC·1 product·🇺🇸 United States

BEAR® (Bridge-Enhanced ACL Repair) Implant

FDA registration

MIACH ORTHOPAEDICS·1 product·🇺🇸 United States

THE 4CIS SPINAL SYSTEM AND 4CIS LOW BACK SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

PHILIPS NM3 RESPIRATORY MONITOR WITH VENTASSIST

FDA 510(k)

FDA Class 2 ·Anesthesiology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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