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
- 1,223
- Deaths
- 0
- Injuries
- 58
- Malfunctions
- 1,165
Reports per year
17518
30819
19120
10821
11122
6623
8524
10425
7526
Source: FDA adverse event reports by year received, 2018–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- File, Pulp Canal, EndodonticEKS629
- Scaler, UltrasonicELC218
- Handpiece, Direct Drive, Ac-PoweredEKX110
- 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.
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