company
Diversatek Healthcare
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-04-29Diversatek Healthcare — Class II recall: Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 18mm-19mm-20mm…
- fda_recall · device_recall2026-04-29Diversatek Healthcare — Class II recall: Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 12mm-13.5mm-15…
- fda_recall · device_recall2026-04-29Diversatek Healthcare — Class II recall: Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator, 6mm-7mm-8mm, RE…
- fda_recall · device_recall2026-04-29Diversatek Healthcare — Class II recall: Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 15mm-16.5mm-18…
Frequently asked questions
- How many FDA warning letters has Diversatek Healthcare received?
- Argus HQ has not recorded an FDA warning letter for Diversatek Healthcare in our current dataset.
- What FDA recalls has Diversatek Healthcare issued?
- Argus HQ has recorded 4 FDA recalls tied to Diversatek Healthcare.
- Is Diversatek Healthcare FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 4 recalls, and 0 approval records for Diversatek Healthcare. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.