Manufacturers of surgical mesh products indicated for the transvaginal repair of pelvic organ prolapse (POP) have been ordered by the Food and Drug Administration (FDA) to stop selling and ...
Manufacturers of surgical mesh products for transvaginal repair of pelvic organ prolapse have been ordered to stop selling and distributing the products in the U.S. The Food and Drug Administration ...
CHICAGO--(BUSINESS WIRE)--Mesh Suture, Inc., d.b.a. MSi, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for DURAMESH™ non-absorbable ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback