510(k) · Cleared
ClearedTeleradpro
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Vidar Systems Corp. · LMA Digitizer, Image, Radiological
Cleared on Oct 7, 2010 as substantially equivalent to K993597 (Vidar Systems Corp., 1999) after a 38-day review. Its family tree reaches back 2 generations to 1993. 1 later device descends from it.
- Decided
- Oct 7, 2010
- Review
- 38 days
- Class
- Class II
- Product code
- LMA
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K933632 (1993). 1 later device descends from it, 1 citing it directly.
- Root · 2 generations backK933632 Medscan 12Vidar Systems Corp. · 1993
- 1 generation backK993597 PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617Vidar Systems Corp. · 1999
- This deviceK102476 TeleradproVidar Systems Corp. · 2010
- Descendant · cites it directly · 0 of its ownK130636 Teleradpro Edge; Teleradpro Edge HD-CCDVidar Systems Corp. · 2013
Most influential descendants
Showing 1 of 1 · See all- K130636Teleradpro Edge; Teleradpro Edge HD-CCDVidar Systems Corp. · 2013 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K933632 | Medscan 12 | Vidar Systems Corp. | 1993 | — |
| −1 | K993597 | PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617 | Vidar Systems Corp. | 1999 | — |
| 0 (this device) | K102476 | Teleradpro | Vidar Systems Corp. | 2010 | — |
| +1 | K130636 | Teleradpro Edge; Teleradpro Edge HD-CCD | Vidar Systems Corp. | 2013 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
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.
Planning a device in LMA? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K993597 | PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617Summary page 1…ication Name: Medical Image Digitizer (21 CER 892.2030) Product Code: LMA Predicate Device: Trade Name: TeIeRADPro Film Digitizers 510(k): K993597 Manufactuter: VIDAR Systems Corporation Device Description: The device consists of a film digitizer with single-film or multi-f… | 1999 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K130636 | Teleradpro Edge; Teleradpro Edge HD-CCD | 2013 | 0 |
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 10.8 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K130636 (Vidar Systems Corp., 2013) has gone furthest, with 0 descendants of its own.
- 2 other devices also cite its predicate K993597.
How does its category compare?
All LMA devicesLMA 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
2026 to Oct 25, outlined.
Median 510(k) review, days · LMA
80in 2013
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LMA
1in 2019
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LMA
1in 2013
MAUDE reports naming product code LMA, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 3 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 2 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 1 |
| 2013 | 3 | 80 | 0 | 1 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 1 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The TeleradPRO film digitizer is intended for making digital copies of medical x-ray films.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K102476 · printed Nov 3, 2026
Cite this page
510(k) Report. “K102476: Teleradpro.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K102476
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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