Davol, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Davol, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Bard® Mesh, Bard Soft Mesh, AQUASENS FLUID MONITORING SYSTEM
50
Total
47
Cleared
0
Denied
Davol, Inc. has 47 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Latest FDA clearance: Jun 2025. Active since 1977.
Browse the FDA 510(k) cleared devices submitted by Davol, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Citech and N.V. Kema.
FDA 510(k) Regulatory Record - Davol, Inc.
50 devices
Cleared
Jun 12, 2025
Bard® Mesh
General & Plastic Surgery
22d
Cleared
Apr 09, 2025
Bard Soft Mesh
General & Plastic Surgery
85d
Cleared
Apr 30, 2003
AQUASENS FLUID MONITORING SYSTEM
Obstetrics & Gynecology
13d
Cleared
Feb 13, 2003
DAVOL ARTHROVENT OUTFLOW TUBING
Orthopedic
15d
Cleared
Jan 22, 2001
COMPOSIX KUGEL MESH, MODEL 0010201,0010202,0010203,0010204,0010205
General & Plastic Surgery
90d
Cleared
Dec 22, 2000
DAVOL X-STREAM LAPAROSCOPIC IRRIGATION SYSTEM, MODELS 5551000, 5552000,...
General & Plastic Surgery
14d
Cleared
Nov 15, 1994
DAVOL ATS
Anesthesiology
575d
Cleared
Jun 14, 1994
DAVOL LAPAROSCOPIC SUCTION IRRIGATION PROBE
Obstetrics & Gynecology
88d
Cleared
Mar 25, 1994
DAVOL SUCTION/IRRIGATOR W/ INTERCHANGEABLE TIP
Obstetrics & Gynecology
731d
Cleared
Mar 07, 1994
DAVOL LAPAROSCOPIC INSUFFLATION TUBING SET
Obstetrics & Gynecology
111d
Cleared
Mar 01, 1994
BARD LAPAROSCOPIC IRRIGATOR PUMP SYSTEM
General & Plastic Surgery
427d
Cleared
Oct 08, 1993
DAVOL CARDIOVASCULAR AUTOTRANSFUSION UNIT
Anesthesiology
193d
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