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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceEmbrace Hydrogel Embolic System (HES)
Generic NameEmbolization Agent, Vascular
ApplicantInstylla, Inc.
201 Burlington Rd.
North Bldg.
Bedford, MA 01730
PMA NumberP250003
Supplement NumberS005
Date Received02/10/2026
Decision Date04/02/2026
Product Code QVG 
Advisory Committee Cardiovascular
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
a new design of the vial holder component of the HES Precursor Kit packaging
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