Atlas FDA

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

Medical Microinstruments, Inc. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K252287Symani Surgical SystemMedical Microinstruments, Inc.2025-11-101100
K251510Symani Surgical SystemMedical Microinstruments, Inc.2025-09-041110
K242368Symani Surgical SystemMedical Microinstruments, Inc.2025-02-071820
K250014Symani Surgical System (820-03830)Medical Microinstruments, Inc.2025-01-27250

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