Resorba Medical GmbH is one of 208 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Resorba Medical GmbH - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Resorba Medical GmbH has 4 FDA 510(k) cleared medical devices. Based in Nuremberg, DE.
Historical record: 4 cleared submissions from 2014 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Resorba Medical GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Resorba Medical GmbH
4 devices
Cleared
Sep 18, 2018
Caprolon
General & Plastic Surgery
123d
Cleared
Nov 02, 2015
PGA RESORBA, PGA RESOQUICK, GLYCOLON
General & Plastic Surgery
319d
Cleared
Oct 29, 2015
MOPYLEN, RESOPREN, SILK, POLYESTER, NYLON, RESOLON, POLYAMIDE PSEUDO, STEEL
General & Plastic Surgery
315d
Cleared
Jun 23, 2014
SUPOLENE
General & Plastic Surgery
59d