NuvoRecalls & reported problems across all models
JJGC Indústria e Comércio de Materiais Dentários S/A. · 54 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6,053
- Deaths reported
- 0
- Injuries reported
- 6,053
- Recalls
- 0
We found 54 models of Nuvo by JJGC Indústria e Comércio de Materiais Dentários S/A. in the FDA's device registry (GUDID). Together they are named in 6,053 adverse event reports in the FDA's MAUDE database, received between Jun 14, 2021 and Sep 28, 2026 — classified as 6,053 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (5,615 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Nuvo problems
Device problems
- Failure to Osseointegrate5,615
- Loss of Osseointegration377
- Adverse Event Without Identified Device or Use Problem45
- Fracture17
- Difficult to Insert1
Patient problems
- No Clinical Signs, Symptoms or Conditions4,002
- Pain1,767
- Unspecified Infection998
- Swelling/ Edema291
- Fibrosis273
- Hemorrhage/Blood Loss/Bleeding206
- Inflammation98
- Fistula84
Nuvo models
54 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Nuvo CD0903015IMPLANT, ENDOSSEOUS, ROOT-FORM518 reports
- Nuvo CD0903008IMPLANT, ENDOSSEOUS, ROOT-FORM350 reports
- Nuvo CD0903016IMPLANT, ENDOSSEOUS, ROOT-FORM335 reports
- Nuvo CD0903014IMPLANT, ENDOSSEOUS, ROOT-FORM323 reports
- Nuvo CD0903002IMPLANT, ENDOSSEOUS, ROOT-FORM283 reports
- Nuvo CD0903022IMPLANT, ENDOSSEOUS, ROOT-FORM270 reports
- Nuvo CD0903009IMPLANT, ENDOSSEOUS, ROOT-FORM269 reports
- Nuvo CD0903017IMPLANT, ENDOSSEOUS, ROOT-FORM228 reports
- Nuvo CD0903003IMPLANT, ENDOSSEOUS, ROOT-FORM219 reports
- Nuvo CD0902008IMPLANT, ENDOSSEOUS, ROOT-FORM192 reports
- Nuvo CD0903010IMPLANT, ENDOSSEOUS, ROOT-FORM185 reports
- Nuvo CD0903023IMPLANT, ENDOSSEOUS, ROOT-FORM184 reports
- Nuvo CD0903001IMPLANT, ENDOSSEOUS, ROOT-FORM179 reports
- Nuvo CD0903007IMPLANT, ENDOSSEOUS, ROOT-FORM179 reports
- Nuvo CD0903021IMPLANT, ENDOSSEOUS, ROOT-FORM172 reports
- Nuvo CD0902009IMPLANT, ENDOSSEOUS, ROOT-FORM154 reports
- Nuvo CD0903013IMPLANT, ENDOSSEOUS, ROOT-FORM145 reports
- Nuvo CD0903029IMPLANT, ENDOSSEOUS, ROOT-FORM144 reports
- Nuvo CD0903028IMPLANT, ENDOSSEOUS, ROOT-FORM137 reports
- Nuvo CD0902014IMPLANT, ENDOSSEOUS, ROOT-FORM130 reports
- Nuvo CD0903024IMPLANT, ENDOSSEOUS, ROOT-FORM115 reports
- Nuvo CD0902010IMPLANT, ENDOSSEOUS, ROOT-FORM112 reports
- Nuvo CD0902007IMPLANT, ENDOSSEOUS, ROOT-FORM106 reports
- Nuvo CD0903004IMPLANT, ENDOSSEOUS, ROOT-FORM91 reports
- Nuvo CD0902013IMPLANT, ENDOSSEOUS, ROOT-FORM85 reports
- Nuvo CD0902015IMPLANT, ENDOSSEOUS, ROOT-FORM83 reports
- Nuvo CD0902002IMPLANT, ENDOSSEOUS, ROOT-FORM80 reports
- Nuvo CD0902016IMPLANT, ENDOSSEOUS, ROOT-FORM77 reports
- Nuvo CD0902003IMPLANT, ENDOSSEOUS, ROOT-FORM75 reports
- Nuvo CD0902019IMPLANT, ENDOSSEOUS, ROOT-FORM57 reports
- Nuvo CD0903031IMPLANT, ENDOSSEOUS, ROOT-FORM56 reports
- Nuvo CD0903020IMPLANT, ENDOSSEOUS, ROOT-FORM54 reports
- Nuvo CD0903030IMPLANT, ENDOSSEOUS, ROOT-FORM54 reports
- Nuvo CD0902001IMPLANT, ENDOSSEOUS, ROOT-FORM49 reports
- Nuvo CD0902020IMPLANT, ENDOSSEOUS, ROOT-FORM48 reports
- Nuvo CD0903027IMPLANT, ENDOSSEOUS, ROOT-FORM45 reports
- Nuvo CD0902011IMPLANT, ENDOSSEOUS, ROOT-FORM41 reports
- Nuvo CD0902004IMPLANT, ENDOSSEOUS, ROOT-FORM38 reports
- Nuvo CD0902022IMPLANT, ENDOSSEOUS, ROOT-FORM27 reports
- Nuvo CD0903018IMPLANT, ENDOSSEOUS, ROOT-FORM27 reports
- Nuvo CD0903011IMPLANT, ENDOSSEOUS, ROOT-FORM25 reports
- Nuvo CD0902021IMPLANT, ENDOSSEOUS, ROOT-FORM22 reports
- Nuvo CD0903025IMPLANT, ENDOSSEOUS, ROOT-FORM18 reports
- Nuvo CD0903005IMPLANT, ENDOSSEOUS, ROOT-FORM17 reports
- Nuvo CD0902017IMPLANT, ENDOSSEOUS, ROOT-FORM14 reports
- Nuvo CD0902005IMPLANT, ENDOSSEOUS, ROOT-FORM12 reports
- Nuvo CD0903012IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- Nuvo CD0902023IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- Nuvo CD0903026IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- Nuvo CD0902012IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- Nuvo CD0903019IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- Nuvo CD0902006IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- Nuvo CD0903006IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- Nuvo CD0903032IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
Recent Nuvo adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922984 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922971 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922969 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922967 ↗InjurySep 28, 2026Loss of Osseointegration
The clinician reports the implant was inserted (b)(6) 2022 in FDI 37. On (b)(6) 2026, loss of osseointegration was verified. The device was forwarded to the manufacturer. There were no patient operative or post-operative complications reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922885 ↗InjurySep 28, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922862 ↗InjurySep 28, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922861 ↗InjurySep 28, 2026Loss of Osseointegration
Patient problems: Fibrosis; Pain
MAUDE report 50922361 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Fibrosis
MAUDE report 50922360 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Pain
MAUDE report 50922359 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Unspecified Infection
MAUDE report 50922278 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Unspecified Infection
MAUDE report 50922277 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Unspecified Infection
MAUDE report 50922275 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Fibrosis
MAUDE report 50922094 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Fibrosis
MAUDE report 50922092 ↗
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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