Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list InspireMD with 6 device recalls. The most recent is a device recall dated May 1, 2026: Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: C….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| May 1, 2026 | Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840Class II · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to | Device recalls |
| May 1, 2026 | Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830Class II · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to | Device recalls |
| May 1, 2026 | CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930Class II · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to | Device recalls |
| May 1, 2026 | CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040Class II · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to | Device recalls |
| May 1, 2026 | Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940Class II · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to | Device recalls |
| May 1, 2026 | CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030Class II · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
