Skip to content

4CIS Dolphin Tlif Cage System Aiin-0105-0200

by Solco Biomedical Company India Private Limited

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840185327833 UDI-DIDate29 May 2026ListedStatusListed GUDID: not 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  • Withdrawn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
4CIS Dolphin Tlif Cage System
Generic Name
Internal spinal fixation procedure kit, reusable
Model / Ref / Catalog
AIIN-0105-0200, 0105-0200
Primary DI / UDI-DI
00840185327833
510(k) Number
FDA Product Code
MAX
GMDN Term
Internal spinal fixation procedure kit, reusable
Device Class
Class II
Regulation Number
888.3080
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
MRI Safety
MR Conditional

Related devices

Cleared under the same submission (K213653)

Show all (12)

Other devices from Solco Biomedical Company India Private Limited

See all devices from Solco Biomedical Company India Private Limited →

Properties

  • Single Use
  • Contains Latex
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No