Trinity Laboratories, Inc. - FDA 510(k) Cleared Devices
44
Total
28
Cleared
0
Denied
Trinity Laboratories, Inc. has 28 FDA 510(k) cleared medical devices. Based in Raleigh, US.
Historical record: 28 cleared submissions from 1990 to 1998.
Browse the FDA 510(k) cleared devices submitted by Trinity Laboratories, Inc. Filter by specialty or product code using the sidebar.
44 devices
Cleared
Jul 10, 1998
HEART CATH TRAY, STERILE, DISPOSABLE
Cardiovascular
80d
Cleared
Feb 04, 1998
DENTAL TRAY, STERILE, DISPOSABLE
Dental
84d
Cleared
Dec 12, 1997
CIRCUMCISION TRAY, CAT. NO. 70340
Obstetrics & Gynecology
28d
Cleared
Aug 01, 1997
CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE...
Immunology
53d
Cleared
Mar 31, 1997
EYE TRAY
General Hospital
32d
Cleared
Feb 14, 1997
O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE
General & Plastic Surgery
50d
Cleared
Jan 22, 1997
BASIC BIOPSY TRAY. DISPOSABLE, STERILE
General & Plastic Surgery
44d
Cleared
Nov 16, 1995
MID-STREAM COLLECTION SET-STERILE
Microbiology
87d
Cleared
Sep 21, 1995
STERILE V.A.D. (VASCULAR ACCESS DEVICES) ACCESS KIT, DISPOSABLE
General Hospital
142d
Cleared
Sep 08, 1995
WOUNDFOAM 4 X 4
General & Plastic Surgery
70d
Cleared
Jul 03, 1995
SUCTION CATHETER KIT, STERILE, SINGLE-USE
Anesthesiology
91d
Cleared
Jun 15, 1995
STANDARD FOLEY SYSTEM PAK
Gastroenterology & Urology
78d
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