510(k) Report

510(k) · Cleared

Cleared

Optyse Ophthalmoscope

K061278510(k) AbbreviatedCleared May 16, 20068-day reviewClass II21 CFR 886.1570

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

Ophthalmos, Ltd. · HLJ Ophthalmoscope, Battery-Powered

Cleared on May 16, 2006 as substantially equivalent to K925756 (Rudolf Riester GmbH & Co. KG, 1993) after an 8-day review. Its family tree reaches back 1 generation to 1993.

Decided
May 16, 2006
Review
8 days
Class
Class II
Product code
HLJ
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K925756 (1993). No later device cites it as a predicate yet.

K925756 · UNI II · Rudolf Riester GmbH & Co. KG · 19931990199520002005
K925756 · UNI II · Rudolf Riester GmbH & Co. KG · 19930
  1. Root · 1 generation backK925756 UNI IIRudolf Riester GmbH & Co. KG · 1993
  2. This deviceK061278 Optyse OphthalmoscopeOphthalmos, Ltd. · 2006
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K925756UNI IIRudolf Riester GmbH & Co. KG1993—
0 (this device)K061278Optyse OphthalmoscopeOphthalmos, Ltd.2006—
FIG. 1 — Lineage of K061278, 1993–2006Source: 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
*K925756UNI II
Summary page 1
…owing cleared device: Company Device 610(k) Rudolf Riester GMBH Uni II K925756 (5) Device Description The Optyse TM is a compact battery-powered handheld direct ophthalmoscope for use by trained…
Rudolf Riester GmbH & Co. KG1993—

Also cleared against K925756: 1 other device →

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?

  • Its one ancestor has no recall.
  • 1 other device also cites its predicate K925756.

How does its category compare?

All HLJ devices

HLJ Ophthalmoscope, Battery-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HLJ

2in 2015

2007: 12010: 12013: 32014: 12015: 2
2007high 3 (2013) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HLJ

140in 2013

2013: 140 days median
2007high 140 (2013)2026

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

Recalls per year · HLJ

No recall names HLJ since 2007.

Adverse event reports per year · HLJ

1in 2023

2020: 12022: 22023: 1
2007high 2 (2022) · low 0 (2007)2025

MAUDE reports naming product code HLJ, 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—00
20080—00
20090—00
20101—00
20110—00
20120—00
2013314000
20141—00
20152—00
20160—00
20170—00
20180—00
20190—00
20200—01
20210—00
20220—02
20230—01
20240—00
20250—00
20260—0—

What is it indicated for?

The Optyse M Lens Free Ophthalmoscope is a direct ophthalmoscope intended to be used to

examine the fundus or the inside of the back of the eye

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K061278: Optyse Ophthalmoscope.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K061278

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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