510(k) Report

510(k) · Cleared

Cleared

Intra Skan DC

K103579510(k) TraditionalCleared Mar 18, 2011102-day reviewClass II21 CFR 872.1800

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

Skanray Technologies · EHD Unit, X-Ray, Extraoral With Timer

Cleared on Mar 18, 2011 as substantially equivalent to K043092 (Progeny, Inc., 2004) and 2 other predicates after a 102-day review. Its family tree reaches back 2 generations to 1994. 2 later devices descend from it.

Decided
Mar 18, 2011
Review
102 days
Class
Class II
Product code
EHD
Recalls
None
Predicates
3

Its longest line of descent runs back 2 generations to K935046 (1994). 3 ancestors in all. 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1999: 1 other ancestor2011: 1 descendant cleared2017: 1 descendant clearedK935046 · GX-770 X-Ray Control, Model 46-404600G4 · Gendex Corp. · 1994K043092 · Preva, 76IN Arm, 66IN Arm, 56IN Arm, Models P7017, P7016, P7015 · Progeny, Inc. · 20041990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant K043092 · Preva, 76IN Arm, 66IN Arm, 56IN Arm, Models P7017, P7016, P7015 · Progeny, Inc. · 2004K935046 · GX-770 X-Ray Control, Model 46-404600G4 · Gendex Corp. · 19940
  1. Root · 2 generations backK935046 GX-770 X-Ray Control, Model 46-404600G4Gendex Corp. · 1994
  2. 1 generation backK043092 Preva, 76IN Arm, 66IN Arm, 56IN Arm, Models P7017, P7016, P7015Progeny, Inc. · 2004
  3. This deviceK103579 Intra Skan DCSkanray Technologies · 2011
  4. Descendant · cites it directly · 1 of its ownK111330 Air Techniques High Frequency Intra-Oral X-RaySkanray Technologies · 2011
  5. Descendant · 2 generations on · 0 of its ownK170967 Intraskan DC PlusSkanray Technologies Private Limited · 2017

Most influential descendants

Showing 2 of 2 · See all
  • K111330Air Techniques High Frequency Intra-Oral X-RaySkanray Technologies · 2011 · cites it directly1descendant
  • K170967Intraskan DC PlusSkanray Technologies Private Limited · 2017 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K935046GX-770 X-Ray Control, Model 46-404600G4Gendex Corp.1994—
−1K043092Preva, 76IN Arm, 66IN Arm, 56IN Arm, Models P7017, P7016, P7015Progeny, Inc.2004—
0 (this device)K103579Intra Skan DCSkanray Technologies2011—
+1K111330Air Techniques High Frequency Intra-Oral X-RaySkanray Technologies2011—
+2K170967Intraskan DC PlusSkanray Technologies Private Limited2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201710
FIG. 1 — Lineage of K103579, 1994–2017Source: 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.

Planning a device in EHD? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new EHD device

  1. #1 K260795 Hand-held Dental X-ray System (HyperLight-M)score 14.1 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (3)

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
*K043092Preva, 76IN Arm, 66IN Arm, 56IN Arm, Models P7017, P7016, P7015
Summary page 1
…e High Frequency Intra Oral X-Ray System -Classification Name 76 EHD - Unit, X-Ray, Extra oral with Timer 5.4 Predicate Device. Progeny PREVA K(043092 Dentsply Gx-770: K(93 5046. Gendex 765DC: K992610. 5.5 Product Description…
Progeny, Inc.2004—
*K935046GX-770 X-Ray Control, Model 46-404600G4Gendex Corp.1994—
*K992610Gendex 765DC, Model 110-0154
Summary page 1
…ification Name 76 EHD - Unit, X-Ray, Extra oral with Timer 5.4 Predicate Device. Progeny PREVA K(043092 Dentsply Gx-770: K(93 5046. Gendex 765DC: K992610. 5.5 Product Description I INTRA SKAN DC is a high frequency…
Dentsply Intl.19994

Also cleared against K043092: 4 other devices →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K111330Air Techniques High Frequency Intra-Oral X-RaySkanray Technologies20111

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 3 companies; a new generation was cleared every 10.8 years on median.
  • 1 of the 3 ancestors has a recall of any class.
  • Of its descendants, K111330 (Skanray Technologies, 2011) has gone furthest, with 1 descendant of its own.
  • 4 other devices also cite its predicate K043092.

How does its category compare?

All EHD devices

EHD Unit, X-Ray, Extraoral With Timer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · EHD

1in 2025

2007: 12008: 52009: 42010: 42011: 32012: 22013: 42014: 32015: 12016: 22017: 42018: 52019: 42020: 22021: 12022: 82023: 82024: 72025: 12026 (partial year): 6
2007high 8 (2022) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EHD

58in 2024

2008: 49 days median2009: 92 days median2010: 268 days median2011: 102 days median2013: 216 days median2014: 107 days median2017: 28 days median2018: 30 days median2019: 173 days median2022: 58 days median2023: 147 days median2024: 58 days median2026 (partial year): 128 days median
2007high 268 (2010) · low 28 (2017)2026

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

Recalls per year · EHD

1in 2017

2010: 32011: 32014: 12016: 12017: 1
2007high 3 (2010) · low 0 (2007)2026

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

Adverse event reports per year · EHD

6in 2024

2007: 52008: 62009: 382010: 472011: 262012: 222013: 212014: 202015: 1102016: 632017: 662018: 212019: 212020: 42021: 42022: 42023: 22024: 6
2007high 110 (2015) · low 0 (2025)2025

MAUDE reports naming product code EHD, 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
20071—05
200854906
2009492038
20104268347
20113102326
20122—022
20134216021
20143107120
20151—0110
20162—163
2017428166
2018530021
20194173021
20202—04
20211—04
202285804
2023814702
202475806
20251—00
202661280—

What is it indicated for?

The INTRA SKAN DC Intraoral Dental X-Ray System is to be used as an extraoral source of X-Rays in Dental radiography.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K103579: Intra Skan DC.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K103579

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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