Dexide, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dexide, Inc. - FDA 510(k) Cleared Devices
38
Total
37
Cleared
0
Denied
Dexide, Inc. has 37 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 37 cleared submissions from 1978 to 1999.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dexide, Inc.
38 devices
Cleared
Jun 23, 1999
MULTACHOICE INSTRUMENTS
General & Plastic Surgery
27d
Cleared
Mar 04, 1999
MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES
General & Plastic Surgery
24d
Cleared
Sep 25, 1998
MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES
General & Plastic Surgery
115d
Cleared
Jul 29, 1998
MULTAPORT CANNULA REDUCER AND ACCESSORIES
General & Plastic Surgery
57d
Cleared
Sep 15, 1995
DEXIDE ENDO-LUBE KIT
General & Plastic Surgery
44d
Cleared
Feb 07, 1995
DEXIDE INSUFFLATION TUBING WITH FILTER
Obstetrics & Gynecology
145d
Cleared
Mar 23, 1993
DEXIDE LAPAROSCOPIC KITS
General & Plastic Surgery
221d
Cleared
Nov 25, 1992
DEXIDE LAPAROSCOPIC ACCESSORIES
General & Plastic Surgery
117d
Cleared
Jul 14, 1992
ENDOBAG, MODIFICATION
General & Plastic Surgery
126d
Cleared
Oct 28, 1991
MONOSCOPY(TM) BRAND, ENDOBAG
General & Plastic Surgery
67d
Cleared
Oct 04, 1991
LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE
General & Plastic Surgery
112d
Cleared
Aug 12, 1991
MONOSCOPY(TM) BRANK, HOOK DISSECTOR
General & Plastic Surgery
46d
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