Tulsa Dental Products LLC
FDA adverse event reports naming Tulsa Dental Products LLC as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: TULSA DENTAL PRODUCTS LLC.
- Total reports
- 1,239
- Deaths
- 0
- Injuries
- 58
- Malfunctions
- 1,181
Reports per year
17518
30819
19120
10821
11122
6623
8524
10425
9126
Source: FDA adverse event reports by year received, 2018–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- File, Pulp Canal, EndodonticEKS644
- Scaler, UltrasonicELC218
- Handpiece, Direct Drive, Ac-PoweredEKX111
- Controller, Foot, Handpiece And CordEBW105
- Resin, Root Canal FillingKIF71
- Handpiece, Contra- And Right-Angle Attachment, DentalEGS37
- Drill, Dental, IntraoralDZA16
- Syringe, Periodontic, Endodontic, IrrigatingEIC11
- Post, Root CanalELR10
- Needle, DentalDZM6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Tulsa Dental Products LLC automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.