Hoya Corporation Pentax Tokyo Office
FDA adverse event reports naming Hoya Corporation Pentax Tokyo Office as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: HOYA CORPORATION PENTAX TOKYO OFFICE.
- Total reports
- 48,217
- Deaths
- 30
- Injuries
- 642
- Malfunctions
- 47,511
Reports per year
114
9315
15116
69917
29718
2,00119
26220
3,56421
12,44722
12,91223
9,52424
4,69925
1,56726
Source: FDA adverse event reports by year received, 2014–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Colonoscope And Accessories, Flexible/RigidFDF19,688
- Gastroscope And Accessories, Flexible/RigidFDS12,616
- Nasopharyngoscope (Flexible Or Rigid)EOB4,633
- Duodenoscope And Accessories, Flexible/RigidFDT3,825
- Bronchoscope (Flexible Or Rigid)EOQ2,703
- Endoscopic Ultrasound System, Gastroenterology-UrologyODG2,425
- Laryngoscope, Non-RigidCAL876
- Endoscope, Accessories, Image Post-Processing For Color EnhancementPEA528
- Cystoscope And Accessories, Flexible/RigidFAJ498
- LaryngostroboscopeEQL140
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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