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Dermal Curette 199-102

by Sontec Instruments, Inc.

Dermal Curette 199-102 is a general-purpose curette (FDA Class I; FDA product code HTF, Curette) made by Sontec Instruments, Inc., listed in FDA GUDID since 14 Aug 2020 (UDI-DI 00192896103870), 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 Number00192896103870 UDI-DI Date14 Aug 2020ListedStatusListed 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  • Withdrawn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
Dermal Curette
Generic name
General-purpose curette
Model / reference
199-102
Primary DI / UDI-DI
00192896103870
FDA product code
HTF
GMDN term
General-purpose curette
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Size
Length — 5.5 Inch

Related devices

Category: General-purpose curette

Similar devices in this category

Other devices filed under General-purpose curette.

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)