Dura substitute: medical device reports filed with FDA

1,404 reports carry this product code, 1996–2026; 0 brands with a page.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

1,404
reports with this product code: 0% of all MAUDE reports; 60
reports, 12 months to August 2026: 51 in the 12 months before; 12.7%
classified as malfunction: 62.3% across all reports; 2.6%
classified as death, as reported: 0.9% across all reports

Product code GXQ is FDA's classification for "Dura substitute" (neurology panel), a class 2 device. 1,404 medical device reports carry this product code, 0% of the MAUDE database, from August 1996 to August 2026.

60 reports arrived in the 12 months to August 2026, up 18% from 51 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are injury (75%), malfunction (12.7%) and other (5.4%). 0 brand names with a page on this site carry this code; the brands table is ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction

Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Integra Lifesciences	356	25.4%
Medtronic Neurosurgery	200	14.2%
Codman & Shurtleff	37	2.6%
Synovis Surgical Innovations	37	2.6%
Cook Biotech	34	2.4%
Integra Neurosciences Pr	34	2.4%
W L Gore & Associates	20	1.4%
Aesculap	9	0.6%
Codman & Shurtleff Medos	5	0.4%
Lifecell	1	0.1%
Mentor	1	0.1%
Raynham	1	0.1%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type and report source

Event type

Death2.6%36

Injury75%1,053

Malfunction12.7%178

Other5.4%76

Not given4.3%61

Who filed

Manufacturer report92.8%1,303

Voluntary report4%56

User facility report0%0

Distributor report0.5%7

Not given2.7%38

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Insufficient device problem information	173	12.3%
Explanted	76	5.4%
Leak/splashthe device leaked	74	5.3%
Fluid/blood leak	45	3.2%
Device remains implanted	38	2.7%
Material disintegration	29	2.1%
Nonstandard device	28	2%
Other (for use when an appropriate device code cannot be identified)	27	1.9%
Replace	26	1.9%
Device operates differently than expectedthe device behaved unexpectedly	24	1.7%
Material puncture/hole	21	1.5%
Product quality problem	21	1.5%
Degraded	17	1.2%
Sterility	16	1.1%
Performance	14	1%
Contamination	13	0.9%
Material integrity problema problem with the device material	13	0.9%
Device appears to trigger rejection	12	0.9%
Improper or incorrect procedure or method	12	0.9%
Lack of effect	12	0.9%

Questions about dura substitute reports

What is product code GXQ?

FDA's classification code for "Dura substitute", class 2, reviewed by the neurology panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,404 reports through August 2026, 60 of them in the latest 12 months.

Which brands appear most often?

No brand with a page on this site.

Can the brands table be used to rank the devices?

No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." Brands differ in how many are in use, how long they have been sold and how reports are collected.

Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.