Device manufacturer, as written on reports

Medos International S Rl: medical device reports filed with FDA

6,783 reports name it as the manufacturer of the device involved, 2017–2026.

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.

6,783
reports naming it as manufacturer: 0% of all MAUDE reports; 1,909
reports, 12 months to August 2026: 1,598 in the 12 months before; 95.6%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

6,783 medical device reports received by FDA give Medos International S Rl as the manufacturer of the device involved, 0% of the MAUDE database, from November 2017 to August 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

1,909 reports arrived in the 12 months to August 2026, up 19% from 1,598 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 (95.6%) and injury (4.4%). 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
Truespan 12 Degree Peek	Fastener, fixation, nondegradable, soft tissue	787	127	0%
Truespan 24 Degree Peek	Fastener, fixation, nondegradable, soft tissue	735	149	0%
4k C-Mnt Scp 4 0 30 167 Mitek	Arthroscope	393	205	0%
Truespan Orthocord	Fastener, fixation, nondegradable, soft tissue	324	381	0%
Rgdloop Adjustable Stnd	Fastener, fixation, nondegradable, soft tissue	312	81	0%
Hd Epscp 4 0 30 167 Mitek	Arthroscope	252	27	0%
Shaver Handpiece 2 0 With Buttons	Arthroscope	231	87	0%
Truespan 24 Degree Plga	Fastener, fixation, nondegradable, soft tissue	212	56	0%
Truespan 12 Degree Plga	Fastener, fixation, nondegradable, soft tissue	198	65	0%
All-In-One Ccu+light Row	Laparoscope, general & plastic surgery	174	75	0%
Camera Head Ac - C-Mount	—	72	25	0%
Fms Vue Pump	Arthroscope	61	37	0%
Truespan Meniscal Repair System Peek 12 Degree	Fastener, fixation, nondegradable, soft tissue	37	0	0%
Truespan Meniscal Repair System Peek 24 Degree	Fastener, fixation, nondegradable, soft tissue	28	0	0%
Inflow Tubing Fms Vue 24pk	Arthroscope	25	22	0%
Micro Tornado Hp W Handcontrol	Arthroscope	23	46	0%
Hd Arthroscope/Sinuscope 4 0mm X 30 Deg X 167mm Mitek Lock	Arthroscope	21	0	0%
UNK - Implant	Fastener, fixation, biodegradable, soft tissue	7	80	0%
4 75 Healix Advance Kntlss Br	Fastener, fixation, biodegradable, soft tissue	1	71	0%
Vapr Vue Generator	Electrosurgical, cutting & coagulation & accessories	1	44	0%

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
MBI	Fastener, fixation, nondegradable, soft tissue	3,069	45.2%
HRX	Arthroscope	1,718	25.3%
MAI	Fastener, fixation, biodegradable, soft tissue	562	8.3%
LXH	Orthopedic manual surgical instrument	410	6%
GCJ	Laparoscope, general & plastic surgery	166	2.4%
FCW	Light source, fiberoptic, routine	150	2.2%
FEM	Accessories, photographic, for endoscope (exclude light sources)	143	2.1%
GAT	Suture, nonabsorbable, synthetic, polyethylene	114	1.7%
NBH	Accessories, arthroscopic	87	1.3%
HWC	Screw, fixation, bone	18	0.3%

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

Death0%0

Injury4.4%300

Malfunction95.6%6,483

Other0%0

Not given0%0

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

Questions about Medos International S Rl reports

How many FDA device reports name Medos International S Rl as manufacturer?

6,783 reports through August 2026, 1,909 of them in the latest 12 months.

Which of its brands appear most often?

Truespan 12 Degree Peek (787), Truespan 24 Degree Peek (735), 4k C-Mnt Scp 4 0 30 167 Mitek (393), Truespan Orthocord (324) and Rgdloop Adjustable Stnd (312).

Which device types does it report on?

fastener, fixation, nondegradable, soft tissue (45.2%), arthroscope (25.3%), fastener, fixation, biodegradable, soft tissue (8.3%) and orthopedic manual surgical instrument (6%).

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.