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

Verite — Predicate Candidate Screening

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

78 daysmedian FDA review time

323 days90th percentile

10clearances measured

K-number	Device	Applicant	Decided	Review days
K844727	MODEL 1000	Verite	1985-07-09	217
K840099	MODEL 800-A VERI/PPR	Verite	1984-11-28	323
K840098	MODEL 811 VERI/TENS & PO	Verite	1984-07-17	189
K822929	VERIL/PPR PERSONAL PAIN RELIEVER #800	Verite	1982-11-17	44
K820651	MODEL 860-1 VERI/PROBE	Verite	1982-04-29	51
K813108	MODEL 500 VERI/500	Verite	1982-02-19	108
K813515	VERI/DFS TM #817	Verite	1982-01-19	35
K811351	VERI-FIER	Verite	1981-07-30	78
K810496	VERI/PMS MODEL 815	Verite	1981-03-13	17
K791187	MODEL 810 VERI/TGS	Verite	1979-08-22	57

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