Crown Delta Corp. is one of 5208 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Crown Delta Corp. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Crown Delta Corp. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 18 cleared submissions from 1976 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Crown Delta Corp. Filter by specialty or product code using the sidebar.
Crown Delta Corp. — FDA 510(k) Products and Clearance History
18 devices
Cleared
May 17, 2013
TRYOUT-VPS HOLDING PASTE
Dental
233d
Cleared
May 14, 2004
CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL
Dental
23d
Cleared
Feb 02, 1996
HEARING AID IMPRESSION MATERIAL
Ear, Nose, Throat
78d
Cleared
Sep 29, 1994
PODIATRIC MATERIAL
Physical Medicine
269d
Cleared
Jan 07, 1994
VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM
Dental
353d
Cleared
Jul 14, 1993
VINYL ADDITION SILICONE SYSTEM
Ear, Nose, Throat
219d
Cleared
Sep 14, 1990
VINYL SILICONE ELASTOMER MATERIAL
General & Plastic Surgery
135d
Cleared
Sep 14, 1990
SILICONE ELASTOMER PUTTY
General & Plastic Surgery
135d
Cleared
Jul 21, 1987
VINYL POLYSILOXANE IMPRESSION SYSTEM
Dental
8d
Cleared
Jun 11, 1987
VINYL POLYSILOXANE IMPRESSION SYSTEM
Dental
64d
Cleared
Oct 18, 1984
TWO COMPONENT RTV VINYL SILICONE MATER
Dental
69d
Cleared
Jun 07, 1982
DENTAL IMPRESSION MATERIAL
Dental
41d