510(k) Report

510(k) · Cleared

Cleared

Heel or Elbow Protector

K812344510(k) TraditionalCleared Sep 11, 198124-day reviewClass I21 CFR 880.6450

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

Fred Sammons, Inc. · FMP Protector, Skin Pressure

Cleared on Sep 11, 1981 after a 24-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Sep 11, 1981
Review
24 days
Class
Class I
Product code
FMP
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2015: 1 descendant cleared19801990200020102020
  1. This deviceK812344 Heel or Elbow ProtectorFred Sammons, Inc. · 1981
  2. Descendant · cites it directly · 0 of its ownK150243 Invictus Medical GelShieldInvictus Medical, Inc. · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K150243Invictus Medical GelShieldInvictus Medical, Inc. · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K812344Heel or Elbow ProtectorFred Sammons, Inc.1981—
+1K150243Invictus Medical GelShieldInvictus Medical, Inc.2015—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
FIG. 1 — Lineage of K812344, 1981–2015Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K150243Invictus Medical GelShieldInvictus Medical, Inc.20150

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?

  • Of its descendants, K150243 (Invictus Medical, Inc., 2015) has gone furthest, with 0 descendants of its own.

How does its category compare?

All FMP devices

FMP Protector, Skin Pressure: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FMP

1in 2015

2015: 1
2007high 1 (2015) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FMP

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

Recalls per year · FMP

1in 2015

2014: 1, 1 Class I2015: 1
2007high 1 (2014) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · FMP

35in 2025

2008: 12009: 72010: 22011: 42012: 72013: 22014: 262015: 92016: 112017: 22018: 12019: 52020: 32021: 42022: 602023: 152024: 102025: 35
2007high 60 (2022) · low 0 (2007)2025

MAUDE reports naming product code FMP, 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—01
20090—07
20100—02
20110—04
20120—07
20130—02
20140—1 (1)26
20151—19
20160—011
20170—02
20180—01
20190—05
20200—03
20210—04
20220—060
20230—015
20240—010
20250—035
20260—0—
Cite this page

510(k) Report. “K812344: Heel or Elbow Protector.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K812344

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026