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Ritter Dental Implant System SAGA-1

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 NumberERITSAGA11 UDI-DIDate4 Aug 2017ListedStatusListed 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  • Withdrawn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 Implant System
Generic Name
Screw endosteal dental implant, two-piece
Model / Reference
SAGA-1
Primary DI / UDI-DI
ERITSAGA11
FDA Product Code
NHA, DZE
GMDN Term
Screw endosteal dental implant, two-piece
Device Class
Class II
Regulation Number
872.3630, 872.3640
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Screw endosteal dental implant, two-piece

Other devices from Ritter Implants GmbH CO KG

See all devices from Ritter Implants GmbH CO KG →

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