510(k) Report

510(k) · Cleared

Cleared

Biopor Aoc Porous Polyethylene, Cerepor

K141880510(k) TraditionalCleared Apr 16, 2015279-day reviewClass II21 CFR 878.3500

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

Ceremed, Inc. · KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

Cleared on Apr 16, 2015 after a 279-day review. The FDA summary names no predicate by number. 2 later devices descend from it.

Decided
Apr 16, 2015
Review
279 days
Class
Class II
Product code
KKY
Recalls
None
Predicates
0

2 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2016: 2 descendants cleared201620182020202220242026
  1. This deviceK141880 Biopor Aoc Porous Polyethylene, CereporCeremed, Inc. · 2015
  2. Descendant · cites it directly · 0 of its ownK161446 Biopor Porous Polyethylene ImplantsCeremed, Inc. · 2016
  3. Descendant · cites it directly · 0 of its ownK160988 Biopor, AOC Porous Polyethylene, CereporCeremed, Inc. · 2016

Most influential descendants

Showing 2 of 2 · See all
  • K161446Biopor Porous Polyethylene ImplantsCeremed, Inc. · 2016 · cites it directly0descendants
  • K160988Biopor, AOC Porous Polyethylene, CereporCeremed, Inc. · 2016 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K141880Biopor Aoc Porous Polyethylene, CereporCeremed, Inc.2015—
+1K161446Biopor Porous Polyethylene ImplantsCeremed, Inc.2016—
+1K160988Biopor, AOC Porous Polyethylene, CereporCeremed, Inc.2016—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201620
FIG. 1 — Lineage of K141880, 2015–2016Source: 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 KKY? 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 KKY device

  1. #1 K211514 Longeviti PorousFit implantscore 2.0 · 2 generations · no Class I recall
Get a 510(k) Report

What was it cleared against?

The FDA summary names no predicate by number.

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K161446Biopor Porous Polyethylene ImplantsCeremed, Inc.20160
K160988Biopor, AOC Porous Polyethylene, CereporCeremed, Inc.20160

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, K161446 (Ceremed, Inc., 2016) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KKY devices

KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · KKY

1in 2021

2007: 12008: 12010: 12011: 12013: 12014: 32015: 12016: 22021: 1
2007high 3 (2014) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KKY

224in 2014

2014: 224 days median
2007high 224 (2014)2026

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

Recalls per year · KKY

1in 2013

2008: 42013: 1
2007high 4 (2008) · low 0 (2007)2026

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

Adverse event reports per year · KKY

1in 2025

2008: 32009: 92010: 52011: 132012: 222013: 172014: 92015: 182016: 252017: 192018: 172019: 202020: 132021: 122022: 12023: 32024: 12025: 1
2007high 25 (2016) · low 0 (2007)2025

MAUDE reports naming product code KKY, 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
20071—00
20081—43
20090—09
20101—05
20111—013
20120—022
20131—117
2014322409
20151—018
20162—025
20170—019
20180—017
20190—020
20200—013
20211—012
20220—01
20230—03
20240—01
20250—01
20260—0—

What is it indicated for?

Biopor® Porous Polyethylene Implants in block, sheet, and anatomical shapes are intended for the augmentation or reconstruction of the maxillofacial skeleton.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K141880: Biopor Aoc Porous Polyethylene, Cerepor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141880

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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