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

Vidar Systems Corp. — Predicate Candidate Screening

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

76 daysmedian FDA review time

151 days90th percentile

13clearances measured

K-number	Device	Applicant	Decided	Review days
K130636	TELERADPRO EDGE; TELERADPRO EDGE HD-CCD	Vidar Systems Corp.	2013-06-07	88
K130406	DIAGNOSTICPRO EDGE	Vidar Systems Corp.	2013-04-29	69
K102476	TELERADPRO	Vidar Systems Corp.	2010-10-07	38
K093809	VIDAR DENTAL FILM DIGITIZER	Vidar Systems Corp.	2010-01-07	29
K071193	VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS	Vidar Systems Corp.	2007-05-30	30
K070563	VIDAR VISION 2000	Vidar Systems Corp.	2007-03-16	17
K024171	VIDAR BONE TRACK SYSTEM SOFTWARE	Vidar Systems Corp.	2003-03-04	76
K011049	EXPRESSSUITE	Vidar Systems Corp.	2001-10-01	178
K993598	MAMMOGRAPHY PRO, MODEL 13017, DIAGNOSTIC PRO W/ MAMMOGRAPHY	Vidar Systems Corp.	2000-01-20	87
K993599	DIAGNOSTIC PRO, MODEL 12772, VXR-16, MODEL 13020, VXR-16 DOS	Vidar Systems Corp.	2000-01-18	85
K993597	PLLL, TELERADPRO, MODEL 12714/12715, VXR-12 PLUS, MODEL 8619	Vidar Systems Corp.	1999-12-15	51
K974315	VIDAR VXR LS LASER FILM DIGITIZER	Vidar Systems Corp.	1998-04-17	151
K933632	MEDSCAN 12	Vidar Systems Corp.	1993-12-13	139

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