PureSperm® 100K

FDA registration

NIDACON INTERNATIONAL AB·1 product·🇸🇪 Sweden

MODIFICATION OF PURESPERM

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Polystar HK

FDA UDI

Merz Dental GmbH·D7091984172·anteriors; shade A3.5; mould 95

Bovie Medical

FDA registration

Industrias Apson S.A de C.V·1 product·🇲🇽 Mexico

Olsen

FDA registration

OLSEN MEDICAL LLC·1 product·🇺🇸 United States

Bovie Medical

FDA registration

ASPEN SURGICAL PRODUCTS, INC.·1 product·🇺🇸 United States

Olsen Medical

FDA registration

Symmetry Surgical Inc.·1 product·🇺🇸 United States

STERILIZATION SERVICES OF GEORGIA, INC.

FDA registration

STERILIZATION SERVICES OF GEORGIA, INC.·1 product·🇺🇸 United States

AccuPlace Round Level Needle Guide

FDA registration

RLS Interventional Inc. DBA Inrad·1 product·🇺🇸 United States

Media, Reproductive

FDA classification

FDA Class 2 ·Media, Reproductive

MODIFIED OLSEN #770 DISPOSABLE HOLSTER

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

ACCUPLACE (TM)

FDA 510(k)

FDA Class 1 ·General, Plastic Surgery

Guide, Needle, Surgical

FDA classification

FDA Class 1 ·Guide, Needle, Surgical

Apparatus, Electrosurgical

FDA classification

FDA Class 2 ·Apparatus, Electrosurgical