510(k) Report

FDA product code · General and plastic surgery

Dressing, Wound And Burn, Interactive

MGRClass IIIPMA required5 decisions since 19967 recalls

5 FDA decisions since 1996. 7 recalls name this code, 0 of them Class I.

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, general and plastic surgery panel

Twenty years of MGR 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 · MGR

3in 2025

2007: 12008: 52009: 62010: 72011: 92012: 92013: 82014: 12016: 32017: 72018: 92019: 122020: 32021: 62022: 62023: 72024: 22025: 32026 (partial year): 2
2007high 12 (2019) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MGR

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

Recalls per year · MGR

2in 2011

2007: 12009: 12010: 12011: 2
2007high 2 (2011) · low 0 (2008)2026

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

Adverse event reports per year · MGR

1in 2020

2007: 22008: 292009: 62010: 32011: 112012: 232013: 182014: 172015: 72016: 32020: 1
2007high 29 (2008) · low 0 (2017)2025

MAUDE reports naming product code MGR, 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—12
20085—029
20096—16
20107—13
20119—211
20129—023
20138—018
20141—017
20150—07
20163—03
20177—00
20189—00
201912—00
20203—01
20216—00
20226—00
20237—00
20242—00
20253—00
20262—0—
FIG. 1 — MGR by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MGR? 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