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Ball Probe 413-026

by Sontec Instruments, Inc.

Ball Probe 413-026 is a Class I device made by Sontec Instruments, Inc., listed in FDA GUDID since 26 Sep 2025 (UDI-DI 00192896122116), 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 Number00192896122116 UDI-DI Date26 Sep 2025ListedStatusListed 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  • Withdrawn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
Ball Probe
Generic name
Open-surgery dissector
Model / Ref / Catalog
413-026
Primary DI / UDI-DI
00192896122116
FDA product code
GDI
GMDN term
Open-surgery dissector
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Dry Heat Sterilization
Size
Length — 9 Inch

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)