Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Modern Medical Equipment Manufacturing, Ltd. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K210315Single Use Hand Switch Monopolar Forceps with Smoke EvacuatiModern Medical Equipment Manufacturing, Ltd.2022-03-174070
K211170Single Use Irrigation bipolar cableModern Medical Equipment Manufacturing, Ltd.2021-10-191830
K200372Smoke Evacuation Fingerswitch, Smoke evacuation system with Modern Medical Equipment Manufacturing, Ltd.2020-11-302900
K192542Foot Control Electrosurgical Pencil, Push Button ElectrosurgModern Medical Equipment Manufacturing, Ltd.2020-06-162740

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