510(k) Report

510(k) · Cleared

Cleared

Periacryl 90,80,70,60, MODEL9010, 8020, 7030, 6040

K071484510(k) TraditionalCleared Oct 10, 2007133-day reviewClass II21 CFR 872.3275

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

Glustitch, Inc. · EMA Cement, Dental

Cleared on Oct 10, 2007 as substantially equivalent to K050658 (Hager Worldwide, Inc., 2005) and 2 other predicates after a 133-day review. Its family tree reaches back 2 generations to 1981. 1 later device descends from it.

Decided
Oct 10, 2007
Review
133 days
Class
Class II
Product code
EMA
Recalls
None
Predicates
3

Its longest line of descent runs back 2 generations to K810545 (1981). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2003: 1 other ancestor1998: 1 other ancestor1988: 1 other ancestor1987: 1 other ancestor2016: 1 descendant clearedK810545 · Pca Periocare Periodontal Dressing · Pulpdent Corp. of America · 1981K050658 · Reso-Pac Periodontal Dressing · Hager Worldwide, Inc. · 200519801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 2 other ancestors 1 generation forward: 1 descendant K050658 · Reso-Pac Periodontal Dressing · Hager Worldwide, Inc. · 2005K810545 · Pca Periocare Periodontal Dressing · Pulpdent Corp. of America · 19810
  1. Root · 2 generations backK810545 Pca Periocare Periodontal DressingPulpdent Corp. of America · 1981
  2. 1 generation backK050658 Reso-Pac Periodontal DressingHager Worldwide, Inc. · 2005
  3. This deviceK071484 Periacryl 90,80,70,60, MODEL9010, 8020, 7030, 6040Glustitch, Inc. · 2007
  4. Descendant · cites it directly · 0 of its ownK142130 Oral BondSteiner Laboratories · 2016

Most influential descendants

Showing 1 of 1 · See all
  • K142130Oral BondSteiner Laboratories · 2016 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K810545Pca Periocare Periodontal DressingPulpdent Corp. of America1981—
−1K050658Reso-Pac Periodontal DressingHager Worldwide, Inc.2005—
0 (this device)K071484Periacryl 90,80,70,60, MODEL9010, 8020, 7030, 6040Glustitch, Inc.2007—
+1K142130Oral BondSteiner Laboratories2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
198810
199810
200310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
FIG. 1 — Lineage of K071484, 1981–2016Source: 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 EMA? 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 EMA device

  1. #1 K254109 G-Cem Universalscore 15.0 · 13 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (3)

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
*K050658Reso-Pac Periodontal Dressing
Summary page 1
…ne 800-667-2130 Facsimile 877-450-4000 Date August 1, 2007 Name Family of PeriAcryl® Classification Dental Cement, 21 CFR 872.3275 Predicate: * K050658 Hager WorldWide, Inc., Hager Reso Pac Periodontal Dressing, market clearance date May 27, 2005;…
Hager Worldwide, Inc.2005—
*K974097Periacryl
Summary page 1
…FR 872.3275 Predicate: * K050658 Hager WorldWide, Inc., Hager Reso Pac Periodontal Dressing, market clearance date May 27, 2005; * K974097 Blacklock Medical Products, Inc., Periacryl, market clearance date April 9, 1998; and * K0305…
Blacklock Medical Products, Inc.1998—
*K030574Gluseal 5ML Dispenser, 1 ML Dispenser, .2 ML Dispenser
Summary page 1
…date May 27, 2005; * K974097 Blacklock Medical Products, Inc., Periacryl, market clearance date April 9, 1998; and * K030574 GluStitch, Inc., GluSeal, market clearance date August 21, 2003. Description The Family of PeriAcryl® is a…
Glustitch, Inc.2003—

Also cleared against K050658: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K142130Oral BondSteiner Laboratories20160

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 26 years and passes through 3 companies; a new generation was cleared every 24.2 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K142130 (Steiner Laboratories, 2016) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K050658.

How does its category compare?

All EMA devices

EMA Cement, Dental: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · EMA

10in 2025

2007: 62008: 132009: 102010: 142011: 82012: 102013: 122014: 42015: 92016: 102017: 32018: 32019: 72020: 82021: 42022: 72023: 22024: 32025: 102026 (partial year): 7
2007high 14 (2010) · low 2 (2023)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EMA

106in 2025

2007: 48 days median2008: 71 days median2009: 86 days median2010: 86 days median2011: 79 days median2012: 128 days median2013: 178 days median2014: 174 days median2015: 134 days median2016: 182 days median2017: 141 days median2018: 237 days median2019: 127 days median2020: 164 days median2021: 184 days median2022: 245 days median2024: 59 days median2025: 106 days median2026 (partial year): 150 days median
2007high 245 (2022) · low 48 (2007)2026

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

Recalls per year · EMA

1in 2023

2008: 22009: 12010: 12011: 52023: 1
2007high 5 (2011) · low 0 (2007)2026

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

Adverse event reports per year · EMA

9in 2025

2007: 332008: 502009: 902010: 1062011: 2242012: 2492013: 3852014: 2072015: 852016: 162017: 132018: 42019: 122020: 52021: 82022: 32023: 62024: 52025: 9
2007high 385 (2013) · low 3 (2022)2025

MAUDE reports naming product code EMA, 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
2007648033
20081371250
20091086190
201014861106
20118795224
2012101280249
2013121780385
201441740207
20159134085
201610182016
20173141013
2018323704
20197127012
2020816405
2021418408
2022724503
20232—16
202435905
20251010609
202671500—

What is it indicated for?

PeriAcryl® 90, PeriAcryl® 80, PeriAcryl® 70, and PeriAcryl® 60 are indicated to be used as an adjunct to temporarily assist in securing periodontal dressings.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071484: Periacryl 90,80,70,60, MODEL9010, 8020, 7030, 6040.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K071484

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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