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Gigli Saw Solid Handle 1100-508

by Sontec Instruments, Inc.

Gigli Saw Solid Handle 1100-508 is a Class I device made by Sontec Instruments, Inc., listed in FDA GUDID since 17 Sep 2018 (UDI-DI 00192896047921), 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 Number00192896047921 UDI-DI Date17 Sep 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  • Withdrawn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
Gigli Saw Solid Handle
Generic name
Manual surgical saw, flexible
Model / Ref / Catalog
1100-508
Primary DI / UDI-DI
00192896047921
FDA product code
GDR
GMDN term
Manual surgical saw, flexible
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Manual surgical saw, flexible

Similar devices

Other devices filed under FDA product code GDR (SAW, MANUAL AND ACCESSORIES).

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)