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Sklar® 17-1260

by Sklar Corporation

Sklar 17-1260 is a surgical soft-tissue manipulation forceps (FDA Class I; FDA product code GEN, Forceps, General & Plastic Surgery) made by Sklar Corporation, listed in FDA GUDID since 25 Apr 2018 (UDI-DI 10649111140198), 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 Number10649111140198 UDI-DI Date25 Apr 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  • Withdrawn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
Sklar®
Generic name
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Model / reference
17-1260
Primary DI / UDI-DI
10649111140198
FDA product code
GEN
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical soft-tissue manipulation forceps, scissors-like, reusable

Similar devices in this category

Other devices filed under Surgical soft-tissue manipulation forceps, scissors-like, reusable.

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Properties

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