"PREVA, 66"" REACH, GRAY W/TWO STUD MOUNT, 12"" CONE"
Model DPD6-G2P · MIDMARK CORPORATION · DI 00841709103872
MUH — System, X-Ray, Extraoral Source, Digital · Class II · 21 CFR 872.1800
UDILibrary device dossier · generated 2026-09-12 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (0)
Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2023-08 | 0 | 2 |
| 2023-10 | 0 | 1 |
| 2026-02 | 0 | 1 |
| 2026-04 | 0 | 1 |
Regulatory clearances
- None linked in the loaded window.
Predicate lineage
K112380 — cites (transitively): K072134 (d1), K090458 (d1)
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — MIDMARK CORPORATION
- Warning Letter 2011-12-28 Midmark Corporation
- Warning Letter 2011-12-28 Midmark Corporation
- NAI 2024-03-14 Midmark Corporation · 0 citations
- VAI 2018-04-02 Midmark Corporation · 1 citations
- VAI 2018-04-02 Midmark Corporation · 1 citations
- NAI 2017-08-22 Midmark Corporation · 0 citations
- NAI 2016-12-09 Midmark Corporation · 0 citations
- NAI 2016-12-09 Midmark Corporation · 0 citations
- VAI 2014-06-09 Midmark Corporation · 8 citations
- VAI 2014-06-09 Midmark Corporation · 8 citations
- VAI 2012-06-28 Midmark Corporation · 4 citations
- VAI 2012-06-28 Midmark Corporation · 4 citations
- VAI 2012-03-13 Midmark Corporation · 2 citations
- OAI 2011-09-12 Midmark Corporation · 8 citations
- OAI 2011-09-12 Midmark Corporation · 8 citations
- VAI 2010-02-24 Midmark Corporation · 2 citations