Medicinelodge, Inc. - FDA 510(k) Cleared Devices
8
Total
6
Cleared
0
Denied
Medicinelodge, Inc. has 6 FDA 510(k) cleared medical devices. Based in Logan, US.
Historical record: 6 cleared submissions from 1996 to 2007. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medicinelodge, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Oct 05, 2007
ZIPKNOT, MODEL 1017-3000
General & Plastic Surgery
28d
Cleared
Jul 27, 2005
MEDICINELODGE ZIPKNOT
General & Plastic Surgery
51d
Cleared
Oct 01, 1996
MLI MODULAR STAPLE
Orthopedic
81d
Cleared
Sep 17, 1996
CROSS PIN
Orthopedic
123d
Cleared
Aug 06, 1996
MEDICINELODGE, INC. SET SCREW
Orthopedic
82d
Cleared
Jul 30, 1996
MLI SOFT TISSUE SCREW & WASHER SYSTEM
Orthopedic
53d
Cleared
Apr 15, 1996
EXPANDED BODY SUTURE
General & Plastic Surgery
32d
Cleared
Jan 30, 1996
MLI INTERFERENCE SCREW
Orthopedic
197d