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Sklar 70-7125

by Sklar Corporation

Sklar 70-7125 is a Class I device made by Sklar Corporation, listed in FDA GUDID since 12 Mar 2019 (UDI-DI 10649111271632), 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 Number10649111271632 UDI-DI Date12 Mar 2019ListedStatusListed 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  • Withdrawn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
Middle ear chisel
Model / reference
70-7125
Primary DI / UDI-DI
10649111271632
FDA product code
FZO
GMDN term
Middle ear chisel
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Middle ear chisel

Similar devices in this category

Other devices filed under Middle ear chisel.

Other devices from Sklar Corporation

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Properties

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