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L10-2® SSIP95103

by Supersonic Imagine, Inc.

L10-2® SSIP95103 is a Class II device made by Supersonic Imagine, Inc., listed in FDA GUDID since 7 Dec 2018 (UDI-DI 03760193600186), 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 Number03760193600186 UDI-DI Date7 Dec 2018ListedStatusListed 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  • Withdrawn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
L10-2®
Generic name
General-purpose ultrasound imaging system
Model / Ref / Catalog
SSIP95103
Primary DI / UDI-DI
03760193600186
FDA product code
ITX, IYN, IYO
GMDN term
General-purpose ultrasound imaging system
Device class
Class II
Regulation number
892.1570, 892.1550, 892.1560
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Length — 250 Centimeter

Related devices

Category: General-purpose ultrasound imaging system

Similar devices in this category

Other devices filed under General-purpose ultrasound imaging system.

Other devices from Supersonic Imagine, Inc.

See all devices from Supersonic Imagine, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)