Atlas FDA

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

Venture Technology, Inc. — Predicate Candidate Screening

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

32 daysmedian FDA review time
88 days90th percentile
5clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K834072INSTRUMENT, DENTALVenture Technology, Inc.1984-02-21880
K822654CURING LIGHTVenture Technology, Inc.1982-10-04320
K812605FIBER OPTIC LIGHT SOURCE IVenture Technology, Inc.1981-10-02170
K790601DENTAL HANDPIECEVenture Technology, Inc.1979-05-31660
K780864DIAMOND STONESVenture Technology, Inc.1978-06-14150

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