510(k) Report

510(k) · Cleared

Cleared

Cirrus HD-Oct

K150977510(k) TraditionalCleared Sep 1, 2015141-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

Carl Zeiss Meditec, Inc. · OBO Tomography, Optical Coherence

Cleared on Sep 1, 2015 as substantially equivalent to K111157 (Carl Zeiss Meditec, Inc., 2012) and 1 other predicate after a 141-day review. Its family tree reaches back 7 generations to 2002. 11 later devices descend from it.

Decided
Sep 1, 2015
Review
141 days
Class
Class II
Product code
OBO
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K012727 (2002). 23 ancestors in all, the oldest K946058 (1995). 11 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor2010: 1 other ancestor2009: 1 other ancestor2007: 1 other ancestor2006: 3 other ancestors2004: 2 other ancestors2002: 2 other ancestors2003: 1 other ancestor2001: 1 other ancestor1998: 1 other ancestor1995: 2 other ancestors2016: 1 descendant cleared2019: 1 descendant cleared2017: 1 descendant cleared2018: 2 descendants cleared2024: 3 descendants cleared2023: 1 descendant cleared2025: 1 descendant cleared2026: 1 descendant clearedK012727 · Humphrey OCT3 · Carl Zeiss Ophthalmic Systems, Inc. · 2002K030433 · Stratusoct with RNFL Normative Database · Carl Zeiss Meditec, Inc. · 2003 · recalledK033123 · Stratusoct with RNFL & Macula Normative Database · Carl Zeiss Meditec, Inc. · 2004 · recalledK063343 · Bioptigen Spectral Domain Ophthalmic Imaging System · Bioptigen, Inc. · 2006K071250 · CA, Model: Cam · Optovue, Inc. · 2007K101505 · Rtvue Model Rtvue 100 · Optovue, Inc. · 2010 · recalledK111157 · CIRRUS HD-OCT WITH RETINAL NERVE FIBER LAYER, MACULAR, OPTIC NERVE HEAD, and GANGLION CELL NORMATIVE DATABASES · Carl Zeiss Meditec, Inc. · 20121995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 3 other ancestors4 generations back: 4 other ancestors5 generations back: 5 other ancestors6 generations back: 1 other ancestor 1 generation forward: 4 descendants2 generations forward: 4 descendants3 generations forward: 3 descendants K111157 · CIRRUS HD-OCT WITH RETINAL NERVE FIBER LAYER, MACULAR, OPTIC NERVE HEAD, and GANGLION CELL NORMATIVE DATABASES · Carl Zeiss Meditec, Inc. · 2012K101505 · Rtvue Model Rtvue 100 · Optovue, Inc. · 2010 · recalledK071250 · CA, Model: Cam · Optovue, Inc. · 2007K063343 · Bioptigen Spectral Domain Ophthalmic Imaging System · Bioptigen, Inc. · 2006K033123 · Stratusoct with RNFL & Macula Normative Database · Carl Zeiss Meditec, Inc. · 2004 · recalledK030433 · Stratusoct with RNFL Normative Database · Carl Zeiss Meditec, Inc. · 2003 · recalledK012727 · Humphrey OCT3 · Carl Zeiss Ophthalmic Systems, Inc. · 2002−50
  1. Root · 7 generations backK012727 Humphrey OCT3Carl Zeiss Ophthalmic Systems, Inc. · 2002
  2. 6 generations backK030433 Stratusoct with RNFL Normative DatabaseCarl Zeiss Meditec, Inc. · 2003 · Recalled
  3. 5 generations backK033123 Stratusoct with RNFL & Macula Normative DatabaseCarl Zeiss Meditec, Inc. · 2004 · Recalled
  4. 4 generations backK063343 Bioptigen Spectral Domain Ophthalmic Imaging SystemBioptigen, Inc. · 2006
  5. 3 generations backK071250 CA, Model: CamOptovue, Inc. · 2007
  6. 2 generations backK101505 Rtvue Model Rtvue 100Optovue, Inc. · 2010 · Recalled
  7. 1 generation backK111157 CIRRUS HD-OCT WITH RETINAL NERVE FIBER LAYER, MACULAR, OPTIC NERVE…Carl Zeiss Meditec, Inc. · 2012
  8. This deviceK150977 Cirrus HD-OctCarl Zeiss Meditec, Inc. · 2015
  9. Descendant · cites it directly · 7 of its ownK161194 PLEX Elite 9000 SS-OCTCarl Zeiss Meditec, Inc. · 2016 · Recalled
  10. Descendant · cites it directly · 6 of its ownK181534 Cirrus HD-OctCarl Zeiss Meditec, Inc. · 2019 · Recalled
  11. Descendant · cites it directly · 2 of its ownK170638 Retina WorkplaceCarl Zeiss Meditec, AG · 2017
  12. Descendant · 2 generations on · 1 of its ownK241081 3D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1 (type: Maestro2); IMAGEnet6…Topcon Corporation · 2024
  13. Descendant · 2 generations on · 1 of its ownK231760 HP-Oct (HP-Oct)Cylite Pty., Ltd. · 2024

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2016: 12017: 12018: 22019: 12023: 12024: 32025: 12026: 1
2016high 3 (2024) · low 0 (2020)2026

Most influential descendants

Showing 5 of 11 · See all
  • K161194PLEX Elite 9000 SS-OCTCarl Zeiss Meditec, Inc. · 2016 · cites it directly7descendants
  • K181534Cirrus HD-OctCarl Zeiss Meditec, Inc. · 2019 · cites it directly6descendants
  • K170638Retina WorkplaceCarl Zeiss Meditec, AG · 2017 · cites it directly2descendants
  • K2410813D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1 (type: Maestro2); IMAGEnet6 Ophthalmic Data…Topcon Corporation · 2024 · 2 generations on1descendant
  • K231760HP-Oct (HP-Oct)Cylite Pty., Ltd. · 2024 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K012727Humphrey OCT3Carl Zeiss Ophthalmic Systems, Inc.2002—
−6K030433Stratusoct with RNFL Normative DatabaseCarl Zeiss Meditec, Inc.20031
−5K033123Stratusoct with RNFL & Macula Normative DatabaseCarl Zeiss Meditec, Inc.20041
−4K063343Bioptigen Spectral Domain Ophthalmic Imaging SystemBioptigen, Inc.2006—
−3K071250CA, Model: CamOptovue, Inc.2007—
−2K101505Rtvue Model Rtvue 100Optovue, Inc.20101
−1K111157CIRRUS HD-OCT WITH RETINAL NERVE FIBER LAYER, MACULAR, OPTIC NERVE HEAD, and…Carl Zeiss Meditec, Inc.2012—
0 (this device)K150977Cirrus HD-OctCarl Zeiss Meditec, Inc.2015—
+1K161194PLEX Elite 9000 SS-OCTCarl Zeiss Meditec, Inc.20161
+1K181534Cirrus HD-OctCarl Zeiss Meditec, Inc.20192
+1K170638Retina WorkplaceCarl Zeiss Meditec, AG2017—
+2K2410813D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1 (type: Maestro2); IMAGEnet6…Topcon Corporation2024—
+2K231760HP-Oct (HP-Oct)Cylite Pty., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199520
199810
200110
200220
200310
200420
200510
200630
200710
200910
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201710
201820
201910
202310
202430
202510
202610
FIG. 1 — Lineage of K150977, 2002–2026Source: 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 OBO? 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 OBO device

  1. #1 K250868 SPECTRALIS HRA+OCT and variantsscore 16.2 · 14 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

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
*K111157CIRRUS HD-OCT WITH RETINAL NERVE FIBER LAYER, MACULAR, OPTIC NERVE HEAD, and GANGLION…
Summary page 4
…rade/Proprietary name: CIRRUS™ HD-OCT PREDICATE DEVICE Company: Carl Zeiss Meditec, Inc. Device: Cirrus™ HD-OCT (K111157) Company: Carl Zeiss Meditec, Inc. Device: Visante OCT (K051789) CARL ZEISS M…
Carl Zeiss Meditec, Inc.2012—
*K051789Visante Oct
Summary page 4
…tec, Inc. Device: Cirrus™ HD-OCT (K111157) Company: Carl Zeiss Meditec, Inc. Device: Visante OCT (K051789) CARL ZEISS MEDITEC, INC. CIRRUS HD-OCT VERSION 8 510(K) PREMARKET NOTIFICA…
Carl Zeiss Meditec, Inc.2005—

Also cleared against K111157: 5 other devices →

What descends from it? (11)

See all 11

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K161194PLEX Elite 9000 SS-OCTCarl Zeiss Meditec, Inc.20167
K181534Cirrus HD-OctCarl Zeiss Meditec, Inc.20196
K170638Retina WorkplaceCarl Zeiss Meditec, AG20172
K182318Retina WorkplaceCarl Zeiss Meditec, Inc.20180

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 13 years and passes through 4 companies; a new generation was cleared every 1.3 years on median.
  • 4 of the 23 ancestors have a recall of any class.
  • Of its descendants, K161194 (Carl Zeiss Meditec, Inc., 2016) has gone furthest, with 7 descendants of its own.
  • 5 other devices also cite its predicate K111157.

How does its category compare?

All OBO devices

OBO Tomography, Optical Coherence: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · OBO

3in 2025

2007: 22008: 22009: 42010: 22011: 22012: 32013: 22014: 32015: 12016: 42017: 42018: 62019: 52020: 22021: 12022: 22023: 72024: 82025: 32026 (partial year): 2
2007high 8 (2024) · low 1 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OBO

125in 2025

2009: 151 days median2012: 269 days median2014: 152 days median2016: 125 days median2017: 118 days median2018: 87 days median2019: 249 days median2023: 262 days median2024: 157 days median2025: 125 days median
2007high 269 (2012) · low 87 (2018)2026

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

Recalls per year · OBO

1in 2022

2010: 12011: 22012: 22018: 12021: 12022: 12026 (partial year): 1
2007high 2 (2011) · low 0 (2007)2026

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

Adverse event reports per year · OBO

4in 2025

2013: 22016: 12018: 12021: 12023: 32024: 32025: 4
2007high 4 (2025) · low 0 (2007)2025

MAUDE reports naming product code OBO, 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
20072—00
20082—00
2009415100
20102—10
20112—20
2012326920
20132—02
2014315200
20151—00
2016412501
2017411800
201868711
2019524900
20202—00
20211—11
20222—10
2023726203
2024815703
2025312504
20262—1—

What is it indicated for?

The CIRRUS™ HD-OCT is a non-contact, high resolution tomographic and biomicroscopic imaging device intended for in-vivo viewing, axial cross-sectional, and three-dimensional imaging of anterior and posterior ocular structures. The device is indicated for visualizing and measuring anterior and posterior ocular structures, including cornea, retina, retinal nerve fiber layer, ganglion cell plus inner plexiform layer, macula, and optic nerve head. The CIRRUS…

Read the full statement (152 words)

The CIRRUS™ HD-OCT is a non-contact, high resolution tomographic and biomicroscopic imaging device intended for in-vivo viewing, axial cross-sectional, and three-dimensional imaging of anterior and posterior ocular structures. The device is indicated for visualizing and measuring anterior and posterior ocular structures, including cornea, retina, retinal nerve fiber layer, ganglion cell plus inner plexiform layer, macula, and optic nerve head. The CIRRUS normative databases are quantitative tools indicated for the comparison of retinal nerve fiber layer thickness, macular thickness, ganglion cell plus inner plexiform layer thickness, and optic nerve head measurements to a database of normal subjects. The CIRRUS OCT angiography is indicated as an aid in the visualization of vascular structures of the retina and choroid. The CIRRUS HD-OCT is indicated as a diagnostic device to aid in the detection and management of ocular diseases including, but not limited to, macular holes, cystoid macular edema, diabetic retinopathy, age-related macular degeneration, and glaucoma.

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. “K150977: Cirrus HD-Oct.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K150977

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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