Aesculap, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ventricular Catheters, Thomale Catheter, Aesculap Aicon® Series Container System, XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set
208
Total
202
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aesculap, Inc. General & Plastic Surgery ✕
71 devices
Cleared
Dec 18, 2020
Aesculap Caiman 12 Seal and Cut Technology System
General & Plastic Surgery
24d
Cleared
Oct 30, 2020
Aesculap Caiman 5 Seal and Cut Technology System
General & Plastic Surgery
30d
Cleared
Sep 02, 2020
Aesculap PAS-Port Proximal Anastomosis System
General & Plastic Surgery
33d
Cleared
Mar 12, 2019
Caiman 5 Maryland
General & Plastic Surgery
113d
Cleared
Mar 07, 2018
Aesculap Optilene Nonabsorbable Suture
General & Plastic Surgery
30d
Cleared
Feb 20, 2018
Aesculap Video Assisted Thoracic Surgery (VATS) INstruments
General & Plastic Surgery
350d
Cleared
Oct 23, 2017
Monosyn Quick Synthetic Absorbable Surgical Suture
General & Plastic Surgery
202d
Cleared
Jun 08, 2017
Novosyn Quick Absorbable Suture
General & Plastic Surgery
97d
Cleared
May 26, 2016
AdTec
General & Plastic Surgery
105d
Cleared
Feb 17, 2016
Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture
General & Plastic Surgery
292d
Cleared
Jul 21, 2015
Caiman Seal and Cut Technology
General & Plastic Surgery
13d
Cleared
Jul 20, 2015
Caiman Seal and Cut Technology
General & Plastic Surgery
27d
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