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Restore L1703-01K

by Keystone Dental Inc.

Restore L1703-01K is a dental drill bit extension (FDA Class II; FDA product code DZI, Drill, Bone, Powered) made by Keystone Dental Inc., listed in FDA GUDID since 8 May 2019 (UDI-DI D768L170301K0), 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 NumberD768L170301K0 UDI-DI Date8 May 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Restore
Generic name
Dental drill bit extension
Model / reference
L1703-01K
Primary DI / UDI-DI
D768L170301K0
FDA product code
DZI
GMDN term
Dental drill bit extension
Device class
Class II
Regulation number
872.4120
GUDID distribution status
In Commercial Distribution

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Category: Dental drill bit extension

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Properties

  • Lot / batch number
Other properties (14, all answered No)