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Companies / InkSpace Imaging
Medical device company profile

InkSpace Imaging

California medical device manufacturer producing lightweight, flexible MRI receive coils for pediatric and adult diagnostic imaging.

Medical Device Manufacturer and DeveloperDiagnostics & ImagingDiagnostic Imaging
HeadquartersπŸ‡ΊπŸ‡ΈPleasanton, California, United States
Founded2016
Commercial statusCommercially availableCommercial flexible MRI receive coils for compatible scanner configurations.
Employees11–50 [12]LinkedIn company-size range Β· Checked 2026-11-04
Estimated revenueNot confirmed
Disclosed fundingUS$10 million [13]Completed Series A reported by the company Β· November 2025
Official websitewww.inkspaceimaging.com β†—

Company overview

InkSpace Imaging is a Pleasanton, California medical device company founded in 2016 and led by President and CEO Peter Fischer. It develops lightweight, flexible MRI receive coils that conform to patient anatomy, with origins in research on printed electronics and magnetic resonance imaging.

Its Snuggle pediatric and Silhouette adult offerings are designed to improve positioning and reduce the handling burden associated with rigid coils. The company supplies configurations for compatible GE HealthCare, Siemens Healthineers and Philips MRI scanners; compatibility depends on the specific coil model, field strength and scanner.

InkSpace began with pediatric imaging and has expanded into adult applications, including musculoskeletal and body imaging. It also develops veterinary configurations. The company reported completing a US$10 million Series A in November 2025 to support expansion of its MRI coil business.

[1][2][3][4][5][6][7][8][9][10][11][12][13]

Leadership

6 people
Peter FischerPresident & Chief Executive Officer [11]
Nabeel EbeidChief Financial Officer [11]
My Nguyen, MSMSEChief Operating Officer [11]
Arvind Kamath, PhDVice President, Engineering [11]
E. Brian Welch, MBA, PhDVice President, Clinical Partnerships [11]
Tracy Wynn, MBAVice President, MR Technology [11]

Products & regulatory status How does MedTechIndex get this information?

Summary

FDA records identify clearances for the Pediatric Body Array, Body Array and Small Body Array configurations. The original Pediatric Body Array decision, K213397, covers pediatric cardiac and body imaging on GE 3.0T systems. Subsequent decisions extend or modify configurations, including adult applications and additional scanner platforms. [1][2][3][4][5]

The most recent identified decision is K262813, dated October 5, 2026, for the Small Body Array SBA12PH15x. Each clearance applies to its named device configuration; a scanner brand or field strength supported by one model should not be assumed for the entire range. [6][6][9][10]

Regulatory snapshot How to read this snapshot

U.S. FDA
6+
510(k) clearances
β€”
De Novo grants
β€”
PMA approvals
β€”
Recall events

Latest recorded source review: 2026-11-04.

Scope: selected product families.

Commercial portfolio snapshot

Documented commercial product families.

InkSpace Snuggle pediatric receive-coil configurations shown on patients of different sizes
Image: InkSpace Imaging
MRI receive coil

Snuggle pediatric MRI coils β†—

Flexible receive-coil arrays designed for pediatric cardiac and body MRI, including neonatal and small-patient configurations. Model selection depends on the scanner platform and field strength. [10][1]

Commercially available Β· Model-specific FDA clearances
InkSpace Silhouette flexible MRI coil array with connectors and body-contouring pads
Image: InkSpace Imaging
MRI receive coil

Silhouette adult MRI coils β†—

Flexible body-conforming receive arrays used for adult musculoskeletal and body imaging on compatible scanner systems. The range includes configurations for GE HealthCare, Siemens Healthineers and Philips platforms. [9][6][5][3][2][4]

Commercially available Β· Model-specific FDA clearances

Activity & Milestones

4 events
2026-10-05 Β· Regulatory

Additional Small Body Array configuration cleared

FDA cleared SBA12PH15x under K262813. [6]

2025-11-21 Β· Funding

US$10 million Series A completion reported

Company confirmed completion of its Series A financing. [13]

2021-12-17 Β· Regulatory

Pediatric Body Array receives FDA clearance

FDA cleared the Pediatric Body Array under K213397. [1]

2016 Β· Company

InkSpace Imaging founded

Company established to develop flexible MRI receive-coil technology. [12]

13 Cited Sources

Accessed 11/04/2026

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