Natural-Knee II Revision Fem Spacer

FDA registration

ZIMMER, INC.·1 product·🇺🇸 United States

NATURAL-KNEE II REVISION FEMORAL SPACER LUGS

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

NATURAL-KNEE II REVISION FEMORAL SPACER LUGS

FDA 510(k)

FDA Class 2 ·Orthopedic

artegral

FDA UDI

Merz Dental GmbH·D7091970498·anteriors; shade BL2; mould BM

Hyper Sal

FDA registration

The Ritedose Corporation·1 product·🇺🇸 United States

Gems Oocyte Retrieval Buffer

FDA registration

HAMILTON THORNE, Inc.·1 product·🇺🇸 United States

Hyper-Sal

FDA registration

PARI RESPIRATORY EQUIPMENT, INC.·1 product·🇺🇸 United States

Hyper Sal

FDA registration

The Ritedose Corporation·1 product·🇺🇸 United States

Gems Oocyte Retrieval Buffer ORB-20

FDA registration

GENEA BIOMEDX Pty Ltd.·1 product·🇦🇺 Australia

ELECTRODE, DEPTH

FDA registration

LISI MEDICAL Remmele·1 product·🇺🇸 United States

Gems Oocyte Retrieval Buffer ORB-20, ORB-50

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

HYPER SAL

FDA 510(k)

FDA Class 2 ·Anesthesiology

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Media, Reproductive

FDA classification

FDA Class 2 ·Media, Reproductive

Nebulizer (Direct Patient Interface)

FDA classification

FDA Class 2 ·Nebulizer (Direct Patient Interface)