510(k) Report

510(k) · Cleared

Cleared

Erchonia Zerona Z-Bed

K220519510(k) TraditionalCleared Mar 24, 202229-day reviewClass II21 CFR 878.5400

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

Erchonia Corporation · OLI Fat Reducing Low Level Laser

Cleared on Mar 24, 2022 as substantially equivalent to K162578 (Erchonia Corporation, 2016) after a 29-day review. Its family tree reaches back 1 generation to 2016.

Decided
Mar 24, 2022
Review
29 days
Class
Class II
Product code
OLI
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K162578 (2016). No later device cites it as a predicate yet.

K162578 · Zerona Z6 OTC · Erchonia Corporation · 201620162018202020222024
K162578 · Zerona Z6 OTC · Erchonia Corporation · 20160
  1. Root · 1 generation backK162578 Zerona Z6 OTCErchonia Corporation · 2016
  2. This deviceK220519 Erchonia Zerona Z-BedErchonia Corporation · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K162578Zerona Z6 OTCErchonia Corporation2016—
0 (this device)K220519Erchonia Zerona Z-BedErchonia Corporation2022—
FIG. 1 — Lineage of K220519, 2016–2022Source: 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 OLI? 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 OLI device

  1. #1 K232977 Biophotas Celluma CONTOURscore 23.5 · 18 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
*K162578Zerona Z6 OTC
Summary page 8
…e Device The Erchonia® Zerona® Z-Bed (Model# JZB) is substantially equivalent to the predicate device, the Erchonia® Zerona® Z6 OTC (Model# SHR) previously cleared under K162578. The Zerona® Z6 OTC is the predecessor to the newly designed Zerona® Z-Bed (subject device), both devices have same the principle…
Erchonia Corporation2016—

Also cleared against K162578: 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 K162578.

How does its category compare?

All OLI devices

OLI Fat Reducing Low Level Laser: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · OLI

3in 2025

2010: 12012: 42013: 32014: 32015: 32016: 22017: 22018: 12020: 32021: 12022: 22023: 22025: 32026 (partial year): 3
2007high 4 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OLI

90in 2025

2012: 93 days median2013: 101 days median2014: 159 days median2015: 90 days median2020: 121 days median2025: 90 days median2026 (partial year): 89 days median
2007high 159 (2014) · low 90 (2015)2026

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

Recalls per year · OLI

No recall names OLI since 2007.

Adverse event reports per year · OLI

2in 2023

2010: 12011: 12013: 42017: 12018: 12019: 32020: 22022: 12023: 2
2007high 4 (2013) · low 0 (2007)2025

MAUDE reports naming product code OLI, 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
20101—01
20110—01
201249300
2013310104
2014315900
201539000
20162—00
20172—01
20181—01
20190—03
2020312102
20211—00
20222—01
20232—02
20240—00
202539000
20263890—

What is it indicated for?

The Zerona@ Z-Bed Laser is indicated for use as a non-invasive dermatological aesthetic treatment for the reduction of

body circumference.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K220519: Erchonia Zerona Z-Bed.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K220519

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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