Anthogyr
Anthogyr holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2024, with 2 FDA device recalls on record.
Top product codes for Anthogyr
FDA recalls by Anthogyr
- Z-2753-2016 — Axiom REG implants Sterile The Axiom REG implants are used as artificial root structures for replacement of missing teeth. They can be used for stabilization of removable prostheses or fixation of single tooth restorations or partial dentures. There are different diameters and different lengths for each diameter.
- Z-2754-2016 — Axiom 2.8 implants Sterile The Axiom REG implants are used as artificial root structures for replacement of missing teeth. They can be used for stabilization of removable prostheses or fixation of single tooth restorations or partial dentures. There are different diameters and different lengths for each diameter.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Anthogyr
- K231072 — Anthogyr FlexiBase® titanium bases for Axiom® BL
- K233264 — Anthogyr INTEGRAL Guided Surgery Cassettes
- K230104 — Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL
- K230680 — Anthogyr Surgical Cassettes
- K160730 — Instrument kits
- K093894 — ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE
- K090676 — MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLES
- K040671 — EROJECT, MINIJECT, SELF ASPIRATING SYRINGES, ASPIRATING SYRINGES, NON ASPIRATING SYRINGES
- K041279 — IMPLANTEO IMPLANTOLOGY MOTOR
- K040674 — IMPLANTOLOGY CONTRA ANGLES, ENDODONTIC CONTRA ANGLES, GENERAL DENTISTRY CONTRA ANGLES
Data sourced from openFDA. This site is unofficial and independent of the FDA.