company
INSPIREMD Inc
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_recall2026-06-17INSPIREMD Inc — Class II recall: CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND…
- fda_recall · device_recall2026-06-17INSPIREMD Inc — Class II recall: CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1…
- fda_recall · device_recall2026-06-17INSPIREMD Inc — Class II recall: Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Num…
- fda_recall · device_recall2026-06-17INSPIREMD Inc — Class II recall: Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog N…
- fda_recall · device_recall2026-06-17INSPIREMD Inc — Class II recall: CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND093…
- fda_recall · device_recall2026-06-17INSPIREMD Inc — Class II recall: Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog N…
Frequently asked questions
- How many FDA warning letters has INSPIREMD Inc received?
- Argus HQ has not recorded an FDA warning letter for INSPIREMD Inc in our current dataset.
- What FDA recalls has INSPIREMD Inc issued?
- Argus HQ has recorded 6 FDA recalls tied to INSPIREMD Inc.
- Is INSPIREMD Inc FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 6 recalls, and 0 approval records for INSPIREMD Inc. 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.