510(k) Report

510(k) · Cleared

Cleared

Vidar Dental Film Digitizer

K093809510(k) TraditionalCleared Jan 7, 201029-day reviewClass II21 CFR 892.2030

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Vidar Systems Corp. · LMA Digitizer, Image, Radiological

Cleared on Jan 7, 2010 as substantially equivalent to K993597 (Vidar Systems Corp., 1999) after a 29-day review. Its family tree reaches back 2 generations to 1993.

Decided
Jan 7, 2010
Review
29 days
Class
Class II
Product code
LMA
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K933632 (1993). No later device cites it as a predicate yet.

  1. Root · 2 generations backK933632 Medscan 12Vidar Systems Corp. · 1993
  2. 1 generation backK993597 PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617Vidar Systems Corp. · 1999
  3. This deviceK093809 Vidar Dental Film DigitizerVidar Systems Corp. · 2010
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K933632Medscan 12Vidar Systems Corp.1993—
−1K993597PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617Vidar Systems Corp.1999—
0 (this device)K093809Vidar Dental Film DigitizerVidar Systems Corp.2010—
FIG. 1 — Lineage of K093809, 1993–2010Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K993597PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617
Summary page 1
…LMA Predicate Device: Trade Name: Vidar Sierra (P1 1 1), TeleRADPro and VXR-12 plus Film Digitizers 510(k): K(993597 Manufacturer: VIDAR Systems Corporation Device Description: The Dental Film Digitizer is a medical device used to convert x-ra…
Vidar Systems Corp.1999—

Also cleared against K993597: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 17 years and passes through 1 company; a new generation was cleared every 10.1 years on median.
  • None of the 2 ancestors has a recall.
  • 2 other devices also cite its predicate K993597.

How does its category compare?

All LMA devices

LMA Digitizer, Image, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · LMA

3in 2013

2009: 12010: 22013: 3
2007high 3 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LMA

80in 2013

2013: 80 days median
2007high 80 (2013)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LMA

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LMA

1in 2013

2008: 32012: 12013: 1
2007high 3 (2008) · low 0 (2007)2025

MAUDE reports naming product code LMA, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—03
20091—00
20102—00
20110—00
20120—01
201338001
20140—00
20150—00
20160—00
20170—00
20180—00
20190—10
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

The VIDAR dental film digitizer is used for making digital copies of x-ray film commonly used in dental practices. Images captured with this device are intended for use in primary, secondary and over-reading applications.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K093809: Vidar Dental Film Digitizer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K093809

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026