ARCH - Quakertown

FDA registration

ARCH - Quakertown·1 product·🇺🇸 United States

Apache

FDA registration

GENESYS SPINE·1 product·🇺🇸 United States

Genesys Spine Apache Cervical Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

AGXO

FDA UDI

Oticon A/S·05707131281548·H150V2, BTE 13 WL 85 TC AGXO

90XL INSTRUMENTATION SYSTEM

FDA registration

MESA LABORATORIES, INC.·1 product·🇺🇸 United States

UltiCare Disposable Pen Needles

FDA registration

ULTI MED, INC.·1 product·🇺🇸 United States

Ophthalmic Speculum

FDA UDI

KATENA PRODUCTS, INC.·00841668100066·TEMPORAL SPECULUM CLOSED WIRE

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167311508120·

TALOS® HA PEEK IBF

FDA UDI

MEDITECH SPINE, LLC·B167321508120·

BD FACSPresto System

FDA registration

Becton, Dickinson and Company, BD Biosciences·4 products·🇺🇸 United States

SSP-SIMATRIX INC.

FDA registration

SSP-SIMATRIX INC.·1 product·🇺🇸 United States

Synergy Health AST, LLC

FDA registration

Synergy Health AST, LLC·1 product·🇺🇸 United States

BD FACSPresto System

FDA registration

Becton Dickinson Caribe, LTD·4 products·🇺🇸 United States

90XL INSTRUMENTATION SYSTEM

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

ULTICARE DISPOSABLE PEN NEEDLES

FDA 510(k)

FDA Class 2 ·General Hospital

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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

Meter, Conductivity, Non-Remote

FDA classification

FDA Class 2 ·Meter, Conductivity, Non-Remote

Needle, Hypodermic, Single Lumen

FDA classification

FDA Class 2 ·Needle, Hypodermic, Single Lumen