Device manufacturer, as written on reports

Ebi: medical device reports filed with FDA

2,842 reports name it as the manufacturer of the device involved, 1997–2026.

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.

2,842
reports naming it as manufacturer: 0% of all MAUDE reports; 155
reports, 12 months to August 2026: 162 in the 12 months before; 23.7%
classified as malfunction: 62.3% across all reports; 0.2%
classified as death, as reported: 0.9% across all reports

2,842 medical device reports received by FDA give Ebi as the manufacturer of the device involved, 0% of the MAUDE database, from January 1997 to August 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

155 reports arrived in the 12 months to August 2026, close to the 162 of 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 (75.4%), malfunction (23.7%) and death (0.2%). 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
Sybronpro Tl	Implant, endosseous, root-form	286	0	0%
Biomet Ebi Bone Healing System	Stimulator, bone growth, non-invasive	248	53	0%
Spinalpak Assembly	Stimulator, bone growth, non-invasive	198	0	1%
Sybronpro Xrt	Implant, endosseous, root-form	181	0	0%
Synergy	Coronary drug-eluting stent	1	84	3.5%

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
LOF	Stimulator, bone growth, non-invasive	1,239	43.6%
DZE	Implant, endosseous, root-form	482	17%
KWQ	Appliance, fixation, spinal intervertebral body	175	6.2%
MNI	Orthosis, spinal pedicle fixation	135	4.8%
HXX	Screwdriver	93	3.3%
KWP	Appliance, fixation, spinal interlaminal	82	2.9%
NKB	Thoracolumbosacral pedicle screw system	74	2.6%
ILO	Pack, hot or cold, water circulating	72	2.5%
MAX	Intervertebral fusion device with bone graft, lumbar	56	2%
HSB	Rod, fixation, intramedullary and accessories	52	1.8%

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

Death0.2%6

Injury75.4%2,142

Malfunction23.7%674

Other0%1

Not given0.7%19

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

Questions about Ebi reports

How many FDA device reports name Ebi as manufacturer?

2,842 reports through August 2026, 155 of them in the latest 12 months.

Which of its brands appear most often?

Sybronpro Tl (286), Biomet Ebi Bone Healing System (248), Spinalpak Assembly (198), Sybronpro Xrt (181) and Synergy (1).

Which device types does it report on?

stimulator, bone growth, non-invasive (43.6%), implant, endosseous, root-form (17%), appliance, fixation, spinal intervertebral body (6.2%) and orthosis, spinal pedicle fixation (4.8%).

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.