J. Jamner Surgical Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
J. Jamner Surgical Instruments, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
J. Jamner Surgical Instruments, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1977 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by J. Jamner Surgical Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - J. Jamner Surgical Instruments, Inc.
11 devices
Cleared
Nov 21, 2008
JARIT HULKA UTERINE TENACULUM FORCEPS
Obstetrics & Gynecology
98d
Cleared
Feb 02, 1995
JARIT RECOMMENDED SINUS INSTRUMENTS
Ear, Nose, Throat
133d
Cleared
Nov 02, 1994
JARIT ENDOSCOPES, MODELS 600-600
General & Plastic Surgery
41d
Cleared
May 16, 1994
JARIT RECOMMENDED SINUS INSTRUMENTS
Ear, Nose, Throat
45d
Cleared
Apr 21, 1994
JARIT SURGICAL INSTRUMENTS
Obstetrics & Gynecology
335d
Cleared
Feb 23, 1994
JARIT SURGICAL INSTRUMENTS: CATALOG 615-330, 615-331, 615-334, 615-335,...
General & Plastic Surgery
205d
Cleared
Nov 10, 1993
JARIT SURGICAL INSTRUMENTS
General & Plastic Surgery
208d
Cleared
Oct 05, 1993
JARIT SURGICAL INSTRUMENTS
General & Plastic Surgery
167d
Cleared
Aug 19, 1993
JARIT ENDOSCOPES, 600-600
General & Plastic Surgery
127d
Cleared
Sep 12, 1977
LEININGEO AORTIC PUNCH #310-395 & 397
Cardiovascular
18d
Cleared
Sep 06, 1977
COPE LUNG FORCEPS #305-218
General & Plastic Surgery
12d