510(k) Report

510(k) · Cleared

Cleared

Natural Cycles

K241006510(k) TraditionalCleared Jul 11, 202490-day reviewClass II21 CFR 884.5370

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

Natural Cycles Nordic AB · PYT Device, Fertility Diagnostic, Contraceptive, Software Application

Cleared on Jul 11, 2024 as substantially equivalent to K231274 (Natural Cycles Nordic AB, 2023) after a 90-day review. Its family tree reaches back 3 generations to 2018.

Decided
Jul 11, 2024
Review
90 days
Class
Class II
Product code
PYT
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to DEN170052 (2018). No later device cites it as a predicate yet.

  1. Root · 3 generations backDEN170052 Natural CyclesNatural Cycles Nordic AB · 2018
  2. 2 generations backK202897 Natural CyclesNatural Cycles Nordic AB · 2021
  3. 1 generation backK231274 Natural CyclesNatural Cycles Nordic AB · 2023
  4. This deviceK241006 Natural CyclesNatural Cycles Nordic AB · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3DEN170052Natural CyclesNatural Cycles Nordic AB2018—
−2K202897Natural CyclesNatural Cycles Nordic AB2021—
−1K231274Natural CyclesNatural Cycles Nordic AB2023—
0 (this device)K241006Natural CyclesNatural Cycles Nordic AB2024—
FIG. 1 — Lineage of K241006, 2018–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 PYT? 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 PYT device

  1. #1 K231274 Natural Cyclesscore 15.2 · 2 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? (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
*K231274Natural Cycles
Summary page 5
…latory Class: II Product Code: PYT (Device, fertility diagnostic, contraceptive, software application) Predicate Device K231274 Natural Cycles The predicate device has not been subject to a design-related recall. Device Descripti…
Natural Cycles Nordic AB2023—

Also cleared against K231274: 2 other devices →

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 6 years and passes through 1 company; a new generation was cleared every 2.2 years on median.
  • None of the 3 ancestors has a recall.
  • 2 other devices also cite its predicate K231274.

How does its category compare?

All PYT devices

PYT Device, Fertility Diagnostic, Contraceptive, Software Application: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · PYT

1in 2025

2018: 12021: 22023: 12024: 12025: 12026 (partial year): 1
2007high 2 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PYT

Too few PYT 510(k)s in any year since 2007 to give a median.

Recalls per year · PYT

No recall names PYT since 2007.

Adverse event reports per year · PYT

2in 2023

2019: 12023: 2
2007high 2 (2023) · low 0 (2007)2025

MAUDE reports naming product code PYT, 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
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20181—00
20190—01
20200—00
20212—00
20220—00
20231—02
20241—00
20251—00
20261—0—

What is it indicated for?

Natural Cycles is a stand-alone software application, intended for women 18 years and older, to monitor their fertility.

Natural Cycles can be used for preventing a pregnancy (contraception) or planning a pregnancy (conception).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K241006: Natural Cycles.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K241006

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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