Atlas FDA

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

Technology Delivery Systems, Inc. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K111480MAXIFLEX - SEMI FLEX SCOPE, 25 TO 65 CMTechnology Delivery Systems, Inc.2012-04-043130
K062725MAXIFLEX-SEMI FLEX SCOPETechnology Delivery Systems, Inc.2006-09-29160
K013300MAXIFLEX FIBER OPTIC ENERGY DELIVERY SYSTEMTechnology Delivery Systems, Inc.2002-04-161950

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