510(k) Report

FDA product code · Dental

Barrier, Animal Source, Intraoral

NPLClass II21 CFR 872.3930510(k) required57 decisions since 20019 recalls

57 FDA decisions since 2001. 510(k) reviews decided 2021–2025 took a median of 248 days (half between 174 and 277). 9 recalls name this code, 0 of them Class I. The most-cited predicate is K050446, named by 17 later devices.

An animal source dental barrier is an animal-derived material device, such as collagen, intended to aid in guided tissue/bone regeneration procedures and to act as a stable barrier for the containment of bone graft materials when placed around implants.

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

FIG. A — Illustration, dental panel

Twenty years of NPL at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · NPL

5in 2025

2007: 12008: 42009: 32010: 22011: 42013: 22014: 52015: 12016: 32017: 32018: 12019: 12020: 22021: 22022: 32023: 22024: 32025: 5
2007high 5 (2014) · low 0 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NPL

132in 2025

2008: 172 days median2009: 193 days median2011: 286 days median2014: 140 days median2016: 184 days median2017: 200 days median2022: 290 days median2024: 263 days median2025: 132 days median
2007high 290 (2022) · low 132 (2025)2026

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

Recalls per year · NPL

6in 2019

2012: 32019: 6
2007high 6 (2019) · low 0 (2007)2026

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

Adverse event reports per year · NPL

39in 2025

2012: 32013: 22014: 32015: 52016: 92017: 182018: 142019: 222020: 82021: 112022: 192023: 52024: 202025: 39
2007high 39 (2025) · low 0 (2007)2025

MAUDE reports naming product code NPL, 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
2008417200
2009319300
20102—00
2011428600
20120—33
20132—02
2014514003
20151—05
2016318409
20173200018
20181—014
20191—622
20202—08
20212—011
20223290019
20232—05
20243263020
20255132039
20260—0—
FIG. 1 — NPL by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NPL? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 872.3930.