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Ritter Dental Implants System TTA-TS-RPR

by Ritter Implants GmbH CO KG GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberERITTTATSRPR1 UDI-DIDate18 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Ritter Dental Implants System
Generic Name
Screw endosteal dental implant, two-piece
Model / Reference
TTA-TS-RPR
Primary DI / UDI-DI
ERITTTATSRPR1
FDA Product Code
NHA
GMDN Term
Screw endosteal dental implant, two-piece
Device Class
Class II
Regulation Number
872.3630
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Ritter Implants GmbH CO KG

See all devices from Ritter Implants GmbH CO KG →

Properties

  • Single Use
  • Implantable
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No