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Endoscopic Forehead Lifter 207-956

by Sontec Instruments, Inc.

Endoscopic Forehead Lifter 207-956 is a Class I device made by Sontec Instruments, Inc., listed in FDA GUDID since 4 Oct 2018 (UDI-DI 00192896026377), 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 Number00192896026377 UDI-DI Date4 Oct 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  • Withdrawn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
Endoscopic Forehead Lifter
Generic name
ENT elevator
Model / Ref / Catalog
207-956
Primary DI / UDI-DI
00192896026377
FDA product code
KAD
GMDN term
ENT elevator
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Size
Length — 6.5 Inch

Related devices

Category: ENT elevator

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)