510(k) Report

510(k) · Cleared

Cleared

Forget - Denture Bonding Liquid

K791576510(k) TraditionalCleared Oct 26, 197970-day reviewClass I21 CFR 872.3410

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

Norcliff Thayer, Inc. · KOL Adhesive, Denture, Carboxymethylcellulose Sodium (32%) And Ethylene-Oxide Homopolymer

Cleared on Oct 26, 1979 after a 70-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Oct 26, 1979
Review
70 days
Class
Class I
Product code
KOL
Recalls
None
Predicates
0

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

FIG. 1 — Lineage of K791576Source: FDA 510(k) database · How lineage is built

Get the monthly Device Review Tracker

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.

Planning a device in KOL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
Get a 510(k) Report

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?

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.

How does its category compare?

All KOL devices

KOL Adhesive, Denture, Carboxymethylcellulose Sodium (32%) And Ethylene-Oxide Homopolymer: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KOL

FDA has decided no KOL device since 2007.

Median 510(k) review, days · KOL

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

Recalls per year · KOL

No recall names KOL since 2007.

Adverse event reports per year · KOL

1in 2025

2007: 182008: 312009: 6102010: 5132011: 2712012: 742013: 352014: 302015: 472016: 12017: 32018: 22019: 32020: 52022: 32024: 22025: 1
2007high 610 (2009) · low 0 (2021)2025

MAUDE reports naming product code KOL, 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—018
20080—031
20090—0610
20100—0513
20110—0271
20120—074
20130—035
20140—030
20150—047
20160—01
20170—03
20180—02
20190—03
20200—05
20210—00
20220—03
20230—00
20240—02
20250—01
20260—0—

More from Norcliff Thayer, Inc.

4 FDA decisions under this applicant name. See the company

  • K890290Brace (Orafix Special)Norcliff Thayer, Inc. · 1989
  • K780174OrabriteNorcliff Thayer, Inc. · 1978
  • K771002Ice BandNorcliff Thayer, Inc. · 1977

Recent decisions in KOL

The KOL category page

  • K884999Hold-Fast Denture AdhesiveIodent, Co. · 1989

https://510kreport.com/device/K791576 · printed Nov 6, 2026

Cite this page

510(k) Report. “K791576: Forget - Denture Bonding Liquid.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K791576

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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