TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167311214250·

Meridian

FDA UDI

SEASPINE ORTHOPEDICS CORPORATION·10889981265748·Trial, 39mm x 27mm x 14mm, 25 Deg

Meridian

FDA UDI

SEASPINE ORTHOPEDICS CORPORATION·10889981246501·Interbody, 39mm x 27mm X 14mm, 25 Deg

Airlife Infant Skin Temp Probe

FDA registration

AirLife Finland Oy·1 product·🇫🇮 Finland

BACT/ALERT FN PLUS

FDA registration

bioMerieux, Inc.·1 product·🇺🇸 United States

UniTip High Resolution Catheter

FDA UDI

Unisensor AG·07640172970386·

MICROSCAN DRIED GRAM-NEGATIVE MIC/COMBO PANEL, B1017 PANEL SERIES

FDA 510(k)

FDA Class 2 ·Microbiology

OLYMPUS LTF-S190-10, OLUMPUS OTV-S190, OLYMPUS CLV-S190

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

VuMesh™

FDA UDI

SEASPINE ORTHOPEDICS CORPORATION·10889981036607·14mm Sq 2.5 Deg End Cap

MaxFuse VBR, 10 (D) x 12 (W) x 45 (H)

FDA UDI

Pioneer Surgical Technology, Inc.·00846468055455·10 (D) x 12 (W) x 45 (H)

Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems

FDA classification

FDA Class 2 ·Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems

Plate, Fixation, Bone

FDA classification

FDA Class 2 ·Plate, Fixation, Bone

Laparoscope, Gynecologic (And Accessories)

FDA classification

FDA Class 2 ·Laparoscope, Gynecologic (And Accessories)