Wells Lamont Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wells Lamont Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Wells Lamont Corp. has 4 FDA 510(k) cleared medical devices. Based in Niles, US.
Historical record: 4 cleared submissions from 1993 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Wells Lamont Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wells Lamont Corp.
4 devices
Cleared
Apr 10, 1995
CUT-TEC OR WELLS LAMONT POLYESTER/WIRE CUT-RESISTANT GLOVE LINER WELLS-TEC,...
General Hospital
195d
Cleared
May 12, 1994
NYLON LINER GLOVES
General Hospital
111d
Cleared
Aug 09, 1993
WELLS LAMONT HANDAGES/MED WRAP DRESSINGS
General & Plastic Surgery
258d
Cleared
Jun 15, 1993
WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS
General Hospital
390d