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Sep 30, 2021

InspireMD Q3 2021 Earnings Report

InspireMD's Q3 2021 financial results were announced, featuring a 9.3% increase in revenue and a 24% YoY revenue growth in CGuardâ„¢ sales.

Key Takeaways

InspireMD reported a 9.3% increase in revenue to $1.071 million for Q3 2021, driven by a 23.8% increase in CGuard EPS sales volume. The company's net loss totaled $4.071 million, or $0.53 per share, compared to a net loss of $2.233 million, or $0.96 per share, for the same period in 2020. Cash, cash equivalents, and short-term bank deposits were $37.1 million as of September 30, 2021.

Revenue increased by 9.3% to $1,071,000 compared to Q3 2020.

CGuard EPS sales volume increased by 23.8% year-over-year.

Gross profit decreased by $206,000 to $92,000.

Net loss for the quarter was $4,071,000, or $0.53 per share.

Total Revenue
$1.07M
Previous year: $980K
+9.3%
EPS
-$0.53
Previous year: -$0.9
-41.1%
CGuard EPS Sales Growth
23.8%
Gross Profit
$92K
Previous year: $298K
-69.1%
Cash and Equivalents
$37.1M
Previous year: $10.9M
+240.9%
Free Cash Flow
-$4.3M
Total Assets
$42.6M
Previous year: $10.9M
+291.5%

InspireMD

InspireMD

InspireMD Revenue by Segment

Forward Guidance

The company anticipates continued progress with reimbursement initiatives and growing global demand for CGuard EPS. They expect the fourth quarter of 2021 to yield additional site approvals and patient enrollments for the U.S. C-Guardians trial and are advancing towards regulatory approvals of two new delivery systems.

Positive Outlook

  • Successful expansion of CGuardâ„¢ into France, representing progress in reimbursement initiatives.
  • Growing global demand from physicians for CGuardâ„¢ when treating CAD.
  • On track trial enrollment levels for the U.S. C-Guardians trial.
  • Expected additional site approvals and patient enrollments in Q4 2021.
  • Advancing toward regulatory approvals of two new delivery systems.

Challenges Ahead

  • Risks associated with market acceptance of existing and new products.
  • Potential for negative clinical trial results or lengthy product delays.
  • Inability to secure regulatory approvals for product sales.
  • Intense competition in the medical device industry.
  • Reliance on single suppliers for certain product components.