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LYNKS Frontalis Sling LSFS-2

by Lynk Solutec Inc.

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

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 Number08800268430111 UDI-DI Date3 Mar 2026ListedStatusListed 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  • Withdrawn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
LYNKS Frontalis Sling
Generic Name
Ptosis sling
Model / Reference
LSFS-2
Primary DI / UDI-DI
08800268430111
FDA Product Code
HNM
GMDN Term
Ptosis sling
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution

Properties

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

Other properties (7)

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