Atlas FDA

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

Xact Robotics, Ltd. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K213759XACT Robotic System, ACE ModelXact Robotics, Ltd.2022-09-232970
K221116XACT ACE Robotic SystemXact Robotics, Ltd.2022-05-13280
K201586XACT Robotic SystemXact Robotics, Ltd.2020-07-09280
K191332XACT Robotic SystemXact Robotics, Ltd.2019-10-031400

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