Atlas FDA

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

Ice Neurosystems, Inc. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K222706iCE-SG2 Subcutaneous Electrode KitIce Neurosystems, Inc.2022-12-06900
K201678iCE-SG Subcutaneous Electrode ArraysIce Neurosystems, Inc.2021-03-082620
K191868iCEWav Neuromonitoring PlatformIce Neurosystems, Inc.2020-03-312630

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