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

Endoscopic Technologies, Inc. — Predicate Candidate Screening

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

113 daysmedian FDA review time
576 days90th percentile
8clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K060101ESTECH AORTIC EASY FLOW CANNULAEndoscopic Technologies, Inc.2006-05-101180
K053326ESTECH COBRA ELECTROSURGICAL UNIT & CABLEEndoscopic Technologies, Inc.2006-01-06360
K053100ESTECH COBRA BIPOLAR SYSTEMEndoscopic Technologies, Inc.2005-12-19460
K946105ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIESEndoscopic Technologies, Inc.1995-04-061130
K945978TUBING, NONINVASIVEEndoscopic Technologies, Inc.1995-01-11340
K945979TROCAR/CANNULAEndoscopic Technologies, Inc.1994-12-21130
K924057DISPOSIBLE ELECTRO COAGULATION PROBEEndoscopic Technologies, Inc.1994-03-115760
K922685TROCARSEndoscopic Technologies, Inc.1993-04-053050

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