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The Tony Feck™ RR3010

by Little Implant Co. GUDID

Withdrawn United States

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810008462904 UDI-DIDate13 May 2019ListedStatusWithdrawn

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
The Tony Feck™
Generic Name
Screw endosteal dental implant, one-piece
Model / Reference
RR3010
Primary DI / UDI-DI
00810008462904
FDA Product Code
DZE
GMDN Term
Screw endosteal dental implant, one-piece
Device Class
Class II
Regulation Number
872.3640
Commercial Distribution
Not in Commercial Distribution

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No