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
- 48,039
- Deaths
- 30
- Injuries
- 640
- Malfunctions
- 47,335
Reports per year
114
9315
15116
69917
29718
2,00119
26220
3,56421
12,44722
12,91223
9,52424
4,69925
1,38926
Source: FDA adverse event reports by year received, 2014–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Colonoscope And Accessories, Flexible/RigidFDF19,618
- Gastroscope And Accessories, Flexible/RigidFDS12,574
- Nasopharyngoscope (Flexible Or Rigid)EOB4,598
- Duodenoscope And Accessories, Flexible/RigidFDT3,819
- Bronchoscope (Flexible Or Rigid)EOQ2,698
- Endoscopic Ultrasound System, Gastroenterology-UrologyODG2,414
- Laryngoscope, Non-RigidCAL873
- Endoscope, Accessories, Image Post-Processing For Color EnhancementPEA526
- Cystoscope And Accessories, Flexible/RigidFAJ497
- LaryngostroboscopeEQL138
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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