Kico Knee Innovation Company vs Philips North America: FDA Enforcement Comparison

Philips North America has been the subject of 355 FDA enforcement/approval records tracked by Argus HQ, compared to 2 for Kico Knee Innovation Company.

Kico Knee Innovation Company: 0 warning letters, 2 recalls, 0 approval records, 0 Form 483s.

Philips North America: 0 warning letters, 355 recalls, 0 approval records, 0 Form 483s.

Side by side

Kico Knee Innovation Company — Warning letters0

Philips North America — Warning letters0

Kico Knee Innovation Company — Recalls2

Philips North America — Recalls355

Kico Knee Innovation Company — Approval records0

Philips North America — Approval records0

Kico Knee Innovation Company — Form 483s0

Philips North America — Form 483s0

Timeline

Kico Knee Innovation Company

Most recent FDA action: June 10, 2026

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Philips North America

Most recent FDA action: July 1, 2026

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Cite this comparison

Pre-formatted for a story, footnote, or reference list:

"Kico Knee Innovation Company vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/kico-knee-innovation-company-vs-philips-north-america

Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗