Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Anthogyr — Predicate Candidate Screening

10 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

133 daysmedian FDA review time
407 days90th percentile
10clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K231072Anthogyr FlexiBase® titanium bases for Axiom® BLAnthogyr2024-01-042650
K233264Anthogyr INTEGRAL Guided Surgery CassettesAnthogyr2023-12-22840
K230104Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit componenAnthogyr2023-10-162760
K230680Anthogyr Surgical CassettesAnthogyr2023-07-111200
K160730Instrument kitsAnthogyr2017-04-274070
K093894ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLEAnthogyr2010-03-03750
K090676MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLESAnthogyr2009-05-22700
K040671EROJECT, MINIJECT, SELF ASPIRATING SYRINGES, ASPIRATING SYRIAnthogyr2004-12-142740
K041279IMPLANTEO IMPLANTOLOGY MOTORAnthogyr2004-09-231330
K040674IMPLANTOLOGY CONTRA ANGLES, ENDODONTIC CONTRA ANGLES, GENERAAnthogyr2004-06-301070

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda