Anthogyr is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Anthogyr - FDA 510(k) Cleared Devices
Recent clearances: Anthogyr FlexiBase® titanium bases for Axiom® BL, Anthogyr INTEGRAL Guided Surgery Cassettes, Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL
10
Total
10
Cleared
0
Denied
Anthogyr has 10 FDA 510(k) cleared dental devices. Based in Sallanches, FR.
Latest FDA clearance: Jan 2024. Active since 2004.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Straumann USA, LLC and The Straumann USA, LLC.
FDA 510(k) Regulatory Record - Anthogyr
10 devices
Cleared
Jan 04, 2024
Anthogyr FlexiBase® titanium bases for Axiom® BL
Dental
265d
Cleared
Dec 22, 2023
Anthogyr INTEGRAL Guided Surgery Cassettes
General Hospital
84d
Cleared
Oct 16, 2023
Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL
Dental
276d
Cleared
Jul 11, 2023
Anthogyr Surgical Cassettes
General Hospital
120d
Cleared
Apr 27, 2017
Instrument kits
General Hospital
407d
Cleared
Mar 03, 2010
ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE
Dental
75d
Cleared
May 22, 2009
MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLES
Dental
70d
Cleared
Dec 14, 2004
EROJECT, MINIJECT, SELF ASPIRATING SYRINGES, ASPIRATING SYRINGES, NON...
Dental
274d
Cleared
Sep 23, 2004
IMPLANTEO IMPLANTOLOGY MOTOR
Dental
133d
Cleared
Jun 30, 2004
IMPLANTOLOGY CONTRA ANGLES, ENDODONTIC CONTRA ANGLES, GENERAL DENTISTRY...
Dental
107d