510(k) Report

FDA product code · Dental

Dental Amalgam

OIVClass II21 CFR 872.3070510(k) required3 decisions since 20080 recalls

3 FDA decisions since 2008. 510(k) reviews decided 2021–2025 took a median of 202 days (half between 202 and 202). No recall names this code.

Dental amalgam is a device that consists of a metallic alloy, such as silver, tin, copper, and zinc, that is mixed with liquid elemental mercury for the direct filling of carious lesions or structural defects in teeth

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 OIV 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 · OIV

1in 2023

2008: 12014: 12023: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OIV

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

Recalls per year · OIV

No recall names OIV since 2007.

Adverse event reports per year · OIV

1in 2024

2008: 102009: 12016: 22017: 12018: 22019: 12020: 12021: 42022: 32023: 82024: 1
2007high 10 (2008) · low 0 (2007)2025

MAUDE reports naming product code OIV, 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
20081—010
20090—01
20100—00
20110—00
20120—00
20130—00
20141—00
20150—00
20160—02
20170—01
20180—02
20190—01
20200—01
20210—04
20220—03
20231—08
20240—01
20250—00
20260—0—
FIG. 1 — OIV by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

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

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Related product codes

Other codes under 21 CFR 872.3070.