510(k) Report

510(k) · Cleared

Cleared

Wee Bell

K221356510(k) TraditionalCleared Feb 2, 2023268-day reviewClass II21 CFR 884.4530

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

Wee Medical · HFX Clamp, Circumcision

Cleared on Feb 2, 2023 as substantially equivalent to K151095 (Novadien Healthcare, 2015) after a 268-day review. Its family tree reaches back 2 generations to 2004.

Decided
Feb 2, 2023
Review
268 days
Class
Class II
Product code
HFX
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K032091 (2004). No later device cites it as a predicate yet.

  1. Root · 2 generations backK032091 Smart Klamp Various by SizeEmergogroup, Inc. · 2004
  2. 1 generation backK151095 Circumplast Circumcision DeviceNovadien Healthcare · 2015
  3. This deviceK221356 Wee BellWee Medical · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K032091Smart Klamp Various by SizeEmergogroup, Inc.2004—
−1K151095Circumplast Circumcision DeviceNovadien Healthcare2015—
0 (this device)K221356Wee BellWee Medical2023—
FIG. 1 — Lineage of K221356, 2004–2023Source: 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 HFX? 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 HFX device

  1. #1 K251687 Konig Bell Circumcision Clampscore 11.2 · 2 generations · no Class I recall
  2. #2 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
*K151095Circumplast Circumcision Device
Summary page 4
…HFX Predicate Device: Legally marketed device to which substantial equivalence is claimed: Circumplast circumcision device (K151095) Device Description The wee BELL is a newborn and infant circumcision device. It is used on males with intact foreskin for the p…
Novadien Healthcare2015—

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 19 years and passes through 3 companies; a new generation was cleared every 11.5 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All HFX devices

HFX Clamp, Circumcision: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · HFX

1in 2023

2007: 22010: 12012: 22013: 12015: 22022: 12023: 12026 (partial year): 1
2007high 2 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HFX

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

Recalls per year · HFX

1in 2024

2011: 32014: 22016: 12019: 22024: 1
2007high 3 (2011) · low 0 (2007)2026

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

Adverse event reports per year · HFX

122in 2025

2007: 172008: 62009: 202010: 212011: 122012: 142013: 162014: 202015: 212016: 1472017: 252018: 132019: 112020: 222021: 52022: 32023: 332024: 1212025: 122
2007high 147 (2016) · low 3 (2022)2025

MAUDE reports naming product code HFX, 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—017
20080—06
20090—020
20101—021
20110—312
20122—014
20131—016
20140—220
20152—021
20160—1147
20170—025
20180—013
20190—211
20200—022
20210—05
20221—03
20231—033
20240—1121
20250—0122
20261—0—

What is it indicated for?

The wee BELL is a newborn and infant circumcision device. It is used on males with intact foreskin for the purpose of performing a circumcision (removal of the foreskin/prepuce). It consists of two components: wee Bell Circumcision device and ligature. The ligature is intended for use with the wee Bell Circumcision device only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K221356: Wee Bell.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K221356

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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