Argen Precious Metals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Argen Precious Metals, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARGI-SATIN OR OPTI0-STAR, 285 SL, ARGELITE 52+
217
Total
217
Cleared
0
Denied
Argen Precious Metals, Inc. has 217 FDA 510(k) cleared dental devices. Based in San Diego, US.
Historical record: 217 cleared submissions from 1989 to 1997.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Argen Precious Metals, Inc.
217 devices
Cleared
Feb 27, 1997
ARGI-SATIN OR OPTI0-STAR
Dental
59d
Cleared
May 20, 1996
285 SL
Dental
42d
Cleared
Apr 25, 1996
ARGELITE 52+
Dental
28d
Cleared
Apr 18, 1996
ARGEDENT 40(GOLD-PALLADIUM-SILVER ALLOY FOR PORCELAIN APPLICATION)
Dental
15d
Cleared
Oct 12, 1995
ARGISTAR 74
Dental
24d
Cleared
Oct 07, 1995
ARGENDENT GIO 86 FR
Dental
19d
Cleared
Oct 07, 1995
SILFREE 80SF+
Dental
19d
Cleared
Oct 07, 1995
ARGESOL 600
Dental
19d
Cleared
Oct 07, 1995
ARGENCO 68M
Dental
19d
Cleared
Oct 07, 1995
ARGISTAR BIO 75PF
Dental
22d
Cleared
Oct 07, 1995
ARGEDENT BIO 87 PF
Dental
22d
Cleared
Oct 07, 1995
SUREFIRE S
Dental
18d
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