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Surpass Elite FDSE32516

by Stryker Corp.

Surpass Elite FDSE32516 is a Class III device made by Stryker Corp., listed in FDA GUDID since 17 Jul 2024 (UDI-DI 07613327582628), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07613327582628 UDI-DI Date17 Jul 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Surpass Elite
Generic name
Bare-metal intracranial vascular stent
Model / Ref / Catalog
FDSE32516
Primary DI / UDI-DI
07613327582628
FDA product code
OUT
GMDN term
Bare-metal intracranial vascular stent
Device class
Class III
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Length — 16.0 Millimeter
Lumen/Inner Diameter — 3.25 Millimeter

Related devices

Category: Bare-metal intracranial vascular stent

Similar devices

Other devices filed under FDA product code OUT (Intracranial aneurysm flow diverter).

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)