Syntex Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Syntex Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Syntex Corp. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1976 to 1992. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Syntex Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Syntex Corp.
10 devices
Cleared
Apr 17, 1992
TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION)
Toxicology
85d
Cleared
Oct 24, 1984
SURGIPRESS SURGICAL LOOP
General & Plastic Surgery
42d
Cleared
Jul 27, 1978
AMALGAM ALLOY
Dental
43d
Cleared
Jun 02, 1978
S-100 CT SCANNER
Radiology
28d
Cleared
Apr 28, 1978
FIBER OPTIC HANDPIECE
Dental
32d
Cleared
Jan 03, 1977
OPUS I OPTION - FIBER OPTIC L SYSTEM
Dental
7d
Cleared
Dec 30, 1976
SYNTEX SYSTEM 6000
Radiology
3d
Cleared
Dec 30, 1976
HI-SENSITIVITY MODE OPTION FOR S60-1A
Radiology
3d
Cleared
Dec 23, 1976
OPTIONS FOR STAR DENTAL OPUS I
Dental
7d
Cleared
Nov 24, 1976
COMPUTERIZED TOMOGRAPHY SCANNER
Radiology
9d