Atlas FDA

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

Modern Medical Equipment Manufacturing Limited · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K170703Single Use Arthroscopic Electrode (with Pencil)Modern Medical Equipment Manufacturing Limited2018-05-314490
K163442Single Use Micro Electrode (Brass with gold plated shaft); SModern Medical Equipment Manufacturing Limited2017-09-282940
K152059Disposable General ElectrodeModern Medical Equipment Manufacturing Limited2016-04-212720
K134006DISPOSABLE LAPAROSCOPIC ELECTRODE, DISPOSABLE LAPAROSCOPIC EModern Medical Equipment Manufacturing Limited2014-11-213290

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