Device manufacturer, as written on reports

Angiomed & Medizintechnik Kg: medical device reports filed with FDA

5,082 reports name it as the manufacturer of the device involved, 2001–2026.

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.

5,082
reports naming it as manufacturer: 0% of all MAUDE reports; 327
reports, 12 months to August 2026: 457 in the 12 months before; 73%
classified as malfunction: 62.3% across all reports; 1.2%
classified as death, as reported: 0.9% across all reports

5,082 medical device reports received by FDA give Angiomed & Medizintechnik Kg as the manufacturer of the device involved, 0% of the MAUDE database, from January 2001 to August 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

327 reports arrived in the 12 months to August 2026, down 28% from 457 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 malfunction (73%), injury (25.8%) and death (1.2%). Manufacturers are required to report events they learn of, so a large manufacturer with many products in use files many reports. 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 named most often

Brand	Device type	Reports	Latest 12 months	Classified as death
Fluency Plus Vascular Stent Graft	System, endovascular graft, arteriovenous (av) dialysis access circuit stenosis treatment	728	64	0.4%
Venovo Venous Stent	Stent, iliac vein	549	74	0.5%
E-Luminexx Vascular Stent	Stent, iliac	457	32	5.1%
Lifestent Solo Vascular Stent System	Stent, superficial femoral artery	390	0	0%
LifeStent 5F Vascular Stent	Stent, superficial femoral artery	332	54	0.6%
Covera Vascular Covered Stent	System, endovascular graft, arteriovenous (av) dialysis access circuit stenosis treatment	328	42	0.3%
LifeStent Vascular Stent	Stent, superficial femoral artery	318	7	2.9%
Lifestent XL Vascular Stent	Stent, superficial femoral artery	265	20	0.7%
Fluency Plus Endovascular Stent Graft	System, endovascular graft, arteriovenous (av) dialysis access circuit stenosis treatment	195	35	0.6%
Lifestent Vascular Stent System	Stent, superficial femoral artery	195	0	0.5%
Fluency Plus Tracheobronchial Stent Graft	Prosthesis, tracheal, expandable	88	0	0%
Flair Endovascular Stent Graft	System, endovascular graft, aortic aneurysm treatment	5	0	0.3%
Lifestream Balloon Expandable Vascular Covered Stent	Iliac covered stent, arterial	1	0	4.4%

Brands with a page on this site, 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."

Device types

Product code	Device type	Reports	Share
NIP	Stent, superficial femoral artery	1,996	39.3%
PFV	System, endovascular graft, arteriovenous (av) dialysis access circuit stenosis treatment	1,492	29.4%
QAN	Stent, iliac vein	607	11.9%
NIO	Stent, iliac	562	11.1%
FGE	Stents, drains and dilators for the biliary ducts	255	5%
JCT	Prosthesis, tracheal, expandable	115	2.3%
GAA	Needle, aspiration and injection, disposable	21	0.4%
KNW	Instrument, biopsy	8	0.2%
FAD	Stent, ureteral	4	0.1%
MIH	System, endovascular graft, aortic aneurysm treatment	3	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

Death1.2%59

Injury25.8%1,312

Malfunction73%3,709

Other0%0

Not given0%2

Grey bar: all 26,136,888 MAUDE reports. Event type is the filer's classification and is not verified by FDA.

Questions about Angiomed & Medizintechnik Kg reports

How many FDA device reports name Angiomed & Medizintechnik Kg as manufacturer?

5,082 reports through August 2026, 327 of them in the latest 12 months.

Which of its brands appear most often?

Fluency Plus Vascular Stent Graft (728), Venovo Venous Stent (549), E-Luminexx Vascular Stent (457), Lifestent Solo Vascular Stent System (390) and LifeStent 5F Vascular Stent (332).

Which device types does it report on?

stent, superficial femoral artery (39.3%), system, endovascular graft, arteriovenous (av) dialysis access circuit stenosis treatment (29.4%), stent, iliac vein (11.9%) and stent, iliac (11.1%).

Does a high count say something about the manufacturer?

Not by itself. Manufacturers must file a report for every event they become aware of, so report volume follows the number of devices in use. 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."

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. Manufacturer names are pooled after company suffixes (Inc., LLC, GmbH and similar) are dropped; names that read as a person rather than an organisation are never published. 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.