Devices › Implant, endosseous, root-form
Device brand name · Scs ipg
Genesis: medical device reports filed with FDA
1,648 reports name it, 1998–2022. Manufacturer given most often on reports: Keystone Dental. Product code DZE.
- 1,648
- device reports naming the brand
- 0% of all MAUDE reports · about 59 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 1.9%
- classified as malfunction
- 0.8% across the product code
- 0.1%
- classified as death, as reported
- 1 reports · not verified by FDA
FDA's MAUDE database holds 1,648 reports that name the brand "Genesis" (scs ipg), received between October 1998 and May 2022; the manufacturer given most often on reports is Keystone Dental. Spellings of one product vary from report to report.
0 reports arrived in the 12 months to August 2026, and none 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 (96.9%), malfunction (1.9%) and other (0.8%); across all implant, endosseous, root-form reports (product code DZE) death is recorded in 0% and malfunction in 0.8%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are failure to osseointegrate (61.1%), loss of osseointegration (21.6%) and device operates differently than expected (2.7%). The patient problems coded most often are failure of implant, pain and osteopenia/ osteoporosis. 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."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 3,924,241 reports carrying product code DZE. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Failure to osseointegrate | 1,007 | 61.1% | 62.8% |
| Loss of osseointegration | 356 | 21.6% | 22.4% |
| Device operates differently than expectedthe device behaved unexpectedly | 45 | 2.7% | 0% |
| Communication or transmission problemthe device could not communicate or transmit | 38 | 2.3% | 0% |
| Explanted | 31 | 1.9% | 0.1% |
| No device output | 25 | 1.5% | 0% |
| Premature end-of-life indicator | 23 | 1.4% | 0% |
| Device displays incorrect message | 18 | 1.1% | 0% |
| Replace | 17 | 1% | 0% |
| Insufficient device problem information | 16 | 1% | 0.2% |
| Low battery | 14 | 0.8% | 0% |
| Component(s), worn | 11 | 0.7% | 0% |
| Device inoperablethe device could not be used | 10 | 0.6% | 0% |
| Battery problema problem with the battery | 8 | 0.5% | 0% |
| Device issuea problem with the device | 5 | 0.3% | 0% |
| Fracturea broken bone | 5 | 0.3% | 1.6% |
| Low impedance | 5 | 0.3% | 0% |
| Breakthe device broke | 4 | 0.2% | 0% |
| Component(s), broken | 4 | 0.2% | 0% |
| Premature discharge of battery | 4 | 0.2% | 0% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Failure of implant | 932 | 56.6% |
| Painpain, site not specified | 247 | 15% |
| Osteopenia/ osteoporosis | 216 | 13.1% |
| Inadequate pain relief | 111 | 6.7% |
| Surgical procedure, repeated | 25 | 1.5% |
| Hospitalization required | 11 | 0.7% |
| Discomfortdiscomfort | 9 | 0.5% |
| Surgical procedure | 9 | 0.5% |
| Sinus perforation | 7 | 0.4% |
| Burning sensationa burning feeling | 6 | 0.4% |
| Device overstimulation of tissue | 6 | 0.4% |
| High blood pressure/ hypertension | 6 | 0.4% |
| Osteolysis | 6 | 0.4% |
| Post operative wound infection | 4 | 0.2% |
| Bacterial infectiona bacterial infection | 3 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Genesis | Product code DZE | All MAUDE reports |
|---|---|---|---|
| Reports | 1,648 | 3,924,241 | 26,136,888 |
| Share of that pool | — | 0% | 0% |
| Classified as death, per 1,000 reports | 1 | 0 | 9 |
| Classified as injury | 96.9% | 99.2% | 36.2% |
| Classified as malfunction | 1.9% | 0.8% | 62.3% |
| Filed by the manufacturer | 99% | 77.7% | 94.9% |
Shares are of reports, not 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."
Other brands with product code DZE
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Biohorizons Dental Implant | 58,732 | 0 | 0% |
| BioHorizons Inc. | 57,020 | 25,536 | 0% |
| NobelActive Internal RP 4.3x10mm | 49,098 | 9,528 | 0% |
| BLT ?4.1mm RC, SLA? 10mm, TiZr, Loxim | 45,650 | 9,677 | 0% |
| NobelParallel CC RP 4.3x10mm | 44,269 | 9,318 | 0% |
| BLT ?4.1mm RC, SLActive? 10mm, TiZr, NTP | 41,672 | 7,531 | 0% |
| Unknown Implant | 39,967 | 1,454 | 0% |
| NobelReplace CC RP 4.3x10mm | 35,946 | 8,166 | 0% |
| NobelReplace CC PMC RP 4.3x10mm | 34,447 | 8,690 | 0% |
| NobelActive Internal RP 4.3x11.5mm | 33,117 | 5,704 | 0% |
| BLT ?3.3mm NC, SLA? 10mm, TiZr, Loxim | 28,648 | 5,695 | 0% |
| BLT ?4.1mm RC, SLA? 10mm, Ti, Loxim | 26,724 | 8,481 | 0% |
| BLT ?3.3mm NC, SLActive? 10mm, TiZr, NTP | 26,540 | 4,680 | 0% |
| NobelActive Internal RP 4.3x13mm | 25,556 | 3,764 | 0% |
| BLT ?4.1mm RC, SLA? 8mm, TiZr, Loxim | 24,772 | 5,978 | 0% |
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." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Genesis reports
How many FDA reports name Genesis?
1,648 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
injury (96.9%), malfunction (1.9%) and other (0.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
failure to osseointegrate (61.1%), loss of osseointegration (21.6%), device operates differently than expected (2.7%), communication or transmission problem (2.3%) and explanted (1.9%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99%) and voluntary reports (0.2%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Genesis was at fault?
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." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
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. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. 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.