510(k) Report

510(k) · Cleared

Cleared

Moorflpi-2 Full-Field Laser Perfusion Imager

K122943510(k) TraditionalCleared Jan 3, 2013101-day reviewClass II21 CFR 870.2120

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

Moor Instruments, Ltd. · DPT Probe, Blood-Flow, Extravascular

Cleared on Jan 3, 2013 as substantially equivalent to K063586 (Moor Instruments, Ltd., 2007) after a 101-day review. Its family tree reaches back 4 generations to 1991. 1 later device descends from it.

Decided
Jan 3, 2013
Review
101 days
Class
Class II
Product code
DPT
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K905232 (1991). 5 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK905232 Moor Laser Blood Flow Monitor MBF3Moor Instruments, Ltd. · 1991
  2. 3 generations backK980383 Mooorldi Laser Doppler ImagerMoor Instruments, Ltd. · 1998
  3. 2 generations backK032841 Moorldi Infrared Laser Doppler Imager, Model MOORLD12-IRMoor Instruments, Ltd. · 2003
  4. 1 generation backK063586 Moorflpi Full-Field Laser Perfusion ImagerMoor Instruments, Ltd. · 2007
  5. This deviceK122943 Moorflpi-2 Full-Field Laser Perfusion ImagerMoor Instruments, Ltd. · 2013
  6. Descendant · cites it directly · 0 of its ownK233076 Laser Speckle Imaging System (RFLSI CZW)Rwd Life Science Co., Ltd. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K233076Laser Speckle Imaging System (RFLSI CZW)Rwd Life Science Co., Ltd. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K905232Moor Laser Blood Flow Monitor MBF3Moor Instruments, Ltd.1991—
−3K980383Mooorldi Laser Doppler ImagerMoor Instruments, Ltd.1998—
−2K032841Moorldi Infrared Laser Doppler Imager, Model MOORLD12-IRMoor Instruments, Ltd.2003—
−1K063586Moorflpi Full-Field Laser Perfusion ImagerMoor Instruments, Ltd.2007—
0 (this device)K122943Moorflpi-2 Full-Field Laser Perfusion ImagerMoor Instruments, Ltd.2013—
+1K233076Laser Speckle Imaging System (RFLSI CZW)Rwd Life Science Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K122943, 1991–2024Source: 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 DPT? 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 DPT device

  1. #1 K233076 Laser Speckle Imaging System (RFLSI CZW)score 8.6 · 5 generations · no Class I recall
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K063586Moorflpi Full-Field Laser Perfusion Imager
Summary page 2
…ssification name: Extravascular blood flow probe (21 CFR 870.2120, Product code DPT) Predicate device: moorELPI Full-Field Laser Perfusion Imager, 5 10(k) number K063586 The moorFLPI-2 is a device to perform non-contact imaging of tissue blood perfusion in the niicrocirculation, for example skin,…
Moor Instruments, Ltd.2007—

Also cleared against K063586: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K233076Laser Speckle Imaging System (RFLSI CZW)Rwd Life Science Co., Ltd.20240

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 22 years and passes through 1 company; a new generation was cleared every 5.9 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K233076 (Rwd Life Science Co., Ltd., 2024) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K063586.

How does its category compare?

All DPT devices

DPT Probe, Blood-Flow, Extravascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · DPT

1in 2024

2007: 32009: 12012: 22013: 32014: 32015: 12016: 12017: 12024: 1
2007high 3 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DPT

201in 2014

2007: 55 days median2013: 108 days median2014: 201 days median
2007high 201 (2014) · low 55 (2007)2026

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

Recalls per year · DPT

22in 2024

2024: 22
2007high 22 (2024) · low 0 (2007)2026

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

Adverse event reports per year · DPT

52in 2025

2007: 52008: 12009: 32010: 32011: 32012: 12014: 52018: 32019: 12020: 32021: 132022: 462023: 212024: 1692025: 52
2007high 169 (2024) · low 0 (2013)2025

MAUDE reports naming product code DPT, 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
200735505
20080—01
20091—03
20100—03
20110—03
20122—01
2013310800
2014320105
20151—00
20161—00
20171—00
20180—03
20190—01
20200—03
20210—013
20220—046
20230—021
20241—22169
20250—052
20260—0—

What is it indicated for?

The moorFLPI-2 Full-Field Laser Perfusion Imager is intended for blood flow measurements in the microcirculation. This device is intended for clinical research use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K122943: Moorflpi-2 Full-Field Laser Perfusion Imager.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122943

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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