510(k) Report

510(k) · Cleared

Cleared

Scican Classic

K984556510(k) TraditionalCleared Feb 9, 199948-day reviewClass I21 CFR 872.6640

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

Scholly Fiberoptic GmbH · EIA Unit, Operative Dental

Cleared on Feb 9, 1999 as substantially equivalent to K981937 (Welch Allyn, Inc., 1998) after a 48-day review. Its family tree reaches back 2 generations to 1994.

Decided
Feb 9, 1999
Review
48 days
Class
Class I
Product code
EIA
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K933671 (1994). No later device cites it as a predicate yet.

  1. Root · 2 generations backK933671 UltracamDental Vision Direct, Inc. · 1994
  2. 1 generation backK981937 Welch Allyn Reveal Intraoral Camera SystemWelch Allyn, Inc. · 1998
  3. This deviceK984556 Scican ClassicScholly Fiberoptic GmbH · 1999
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K933671UltracamDental Vision Direct, Inc.1994—
−1K981937Welch Allyn Reveal Intraoral Camera SystemWelch Allyn, Inc.1998—
0 (this device)K984556Scican ClassicScholly Fiberoptic GmbH1999—
FIG. 1 — Lineage of K984556, 1994–1999Source: 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 EIA? 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 EIA device

  1. #1 K231845 Dental unit Model: Marescore 14.4 · 6 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? (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
*K981937Welch Allyn Reveal Intraoral Camera System
Summary page 1
…mon Name - Video Camera System and Accessories Classification Name - Unit, Operative Dental Predicate Device: Welch Allyn Reveal Intraoral Camera System {510(k) number K981937] The purpose of the SciCan Classic and accessories is to provide video images of the mouth and oral structures, dental cavities,…
Welch Allyn, Inc.1998—

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 5 years and passes through 3 companies; a new generation was cleared every 4.4 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All EIA devices

EIA Unit, Operative Dental: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EIA

7in 2025

2007: 32008: 62009: 32010: 32011: 52012: 22013: 22014: 22015: 72016: 42017: 12018: 22019: 22020: 12022: 32023: 32024: 32025: 72026 (partial year): 2
2007high 7 (2015) · low 0 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EIA

178in 2025

2007: 90 days median2008: 72 days median2009: 109 days median2010: 270 days median2011: 150 days median2015: 214 days median2016: 182 days median2022: 265 days median2023: 686 days median2024: 251 days median2025: 178 days median
2007high 686 (2023) · low 72 (2008)2026

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

Recalls per year · EIA

1in 2013

2012: 12013: 1
2007high 1 (2012) · low 0 (2007)2026

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

Adverse event reports per year · EIA

47in 2025

2010: 22011: 32012: 72013: 62014: 2552015: 4522016: 1512017: 642018: 732019: 682020: 482021: 492022: 442023: 532024: 532025: 47
2007high 452 (2015) · low 0 (2007)2025

MAUDE reports naming product code EIA, 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
200739000
200867200
2009310900
2010327002
2011515003
20122—17
20132—16
20142—0255
201572140452
201641820151
20171—064
20182—073
20192—068
20201—048
20210—049
20223265044
20233686053
20243251053
20257178047
20262—0—

What is it indicated for?

The SciCan Classic and accessories are indicated for use when video images are desired to provide visual information during dental examinations and procedures.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K984556: Scican Classic.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K984556

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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