510(k) Report

510(k) · Cleared

Cleared

Pre-Formed Penile Silicone Block

K220760510(k) TraditionalCleared May 13, 202259-day reviewClass II21 CFR 874.3620

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

International Medical Devices, Inc. · MIB Elastomer, Silicone Block

Cleared on May 13, 2022 as substantially equivalent to K181387 (International Medical Devices, Inc., 2019) after a 59-day review. Its family tree reaches back 3 generations to 2002. 1 later device descends from it.

Decided
May 13, 2022
Review
59 days
Class
Class II
Product code
MIB
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K021839 (2002). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 2 other ancestors2002: 1 other ancestor2023: 1 descendant clearedK021839 · Aart Gluteal Implant · Aesthetic and Reconstructive Technologies, Inc. · 2002 · recalledK162624 · Pre-Formed Penile Silicone Block · International Medical Devices, Inc. · 2017K181387 · Pre-Formed Penile Silicone Block · International Medical Devices, Inc. · 2019200020052010201520202025
  1. Root · 3 generations backK021839 Aart Gluteal ImplantAesthetic and Reconstructive Technologies, Inc. · 2002 · Recalled
  2. 2 generations backK162624 Pre-Formed Penile Silicone BlockInternational Medical Devices, Inc. · 2017
  3. 1 generation backK181387 Pre-Formed Penile Silicone BlockInternational Medical Devices, Inc. · 2019
  4. This deviceK220760 Pre-Formed Penile Silicone BlockInternational Medical Devices, Inc. · 2022
  5. Descendant · cites it directly · 0 of its ownK223051 Pre-Formed Silicone BlockInternational Medical Devices, Inc. · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K223051Pre-Formed Silicone BlockInternational Medical Devices, Inc. · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K021839Aart Gluteal ImplantAesthetic and Reconstructive Technologies, Inc.20021
−2K162624Pre-Formed Penile Silicone BlockInternational Medical Devices, Inc.2017—
−1K181387Pre-Formed Penile Silicone BlockInternational Medical Devices, Inc.2019—
0 (this device)K220760Pre-Formed Penile Silicone BlockInternational Medical Devices, Inc.2022—
+1K223051Pre-Formed Silicone BlockInternational Medical Devices, Inc.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210
200420

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
FIG. 1 — Lineage of K220760, 2002–2023Source: 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 MIB? 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 MIB device

  1. #1 K241150 MISTI Silicone Implantscore 8.0 · 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
*K181387Pre-Formed Penile Silicone Block
Summary page 4
…e Name / Manufacturer Primary Number Predicate K181387 Pre-Formed Penile Silicone Block / International Medical Devices, Inc.  DEVICE DESCRIPTION The Pre-Formed Penile Si…
International Medical Devices, Inc.2019—

Also cleared against K181387: 2 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K223051Pre-Formed Silicone BlockInternational Medical Devices, Inc.20230

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 20 years and passes through 2 companies; a new generation was cleared every 3.3 years on median.
  • 2 of the 6 ancestors have a recall of any class.
  • Of its descendants, K223051 (International Medical Devices, Inc., 2023) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K181387.

How does its category compare?

All MIB devices

MIB Elastomer, Silicone Block: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · MIB

1in 2024

2017: 12018: 12019: 12020: 12022: 32023: 12024: 1
2007high 3 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MIB

102in 2022

2022: 102 days median
2007high 102 (2022)2026

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

Recalls per year · MIB

3in 2025

2025: 3
2007high 3 (2025) · low 0 (2007)2026

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

Adverse event reports per year · MIB

18in 2025

2010: 22011: 12012: 22014: 12015: 22016: 12017: 12018: 102019: 32020: 12021: 52022: 192023: 742024: 322025: 18
2007high 74 (2023) · low 0 (2007)2025

MAUDE reports naming product code MIB, 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—02
20110—01
20120—02
20130—00
20140—01
20150—02
20160—01
20171—01
20181—010
20191—03
20201—01
20210—05
20223102019
20231—074
20241—032
20250—318
20260—0—

What is it indicated for?

The Pre-Formed Penile Silicone Block is intended for use in augmentation, reconstructive and cosmetic surgery, and is contoured at the surgeon's discretion to create a custom implant. When used in augmentation procedures, the device provides cosmetic augmentation of the penis and is intended for aesthetic purposes.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K220760: Pre-Formed Penile Silicone Block.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K220760

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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