Atlantis Components, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atlantis Components, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Atlantis Components, Inc. has 18 FDA 510(k) cleared dental devices. Based in Skokie, US.
Historical record: 18 cleared submissions from 1999 to 2011.
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 - Atlantis Components, Inc.
18 devices
Cleared
Feb 03, 2011
ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT
Dental
114d
Cleared
Feb 29, 2008
ATLANTIS ABUTMENT IN ZIRCONIA FOR BIOHORIZONS IMPLANT
Dental
73d
Cleared
Feb 14, 2008
ATLANTIS ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI ABUTMENT FOR...
Dental
86d
Cleared
Nov 16, 2007
ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN MICROAMINI IMPLANTS, GEMINI...
Dental
73d
Cleared
Oct 05, 2007
ATLANTIS, GEMINI AND GEMINI+ ABUTMENTS IN ZIRCONIA FOR ASTRA IMPLANTS
Dental
84d
Cleared
Jun 22, 2007
ATLANTIS ABUTMENT FOR ASTRA IMPLANT
Dental
87d
Cleared
Mar 02, 2007
ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE
Dental
74d
Cleared
Feb 28, 2007
ATLANTIS ABUTMENT FOR 3I CERTAIN MICRO MINI
Dental
211d
Cleared
Feb 14, 2007
ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT
Dental
208d
Cleared
Dec 20, 2006
ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE
Dental
135d
Cleared
Jul 31, 2006
ATLANTIS ABUTMENT FOR NOBEL REPLACE INTERFACE
Dental
213d
Cleared
Jun 30, 2006
ATLANTIS ABUTMENT FOR ZIMMER INTERFACE
Dental
207d