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Safe N Simple LLC SNS00517

by Safe N Simple LLC

Safe N Simple LLC SNS00517 is a Class I device made by Safe N Simple LLC, listed in FDA GUDID since 14 Oct 2026 (UDI-DI 00810040135538), registry data as of 2 Nov 2026.

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

Source GUDID, synced 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810040135538 UDI-DI Date14 Oct 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Safe N Simple LLC
Generic name
Patient medical adhesive remover
Model / Ref / Catalog
SNS00517
Primary DI / UDI-DI
00810040135538
FDA product code
KOX
GMDN term
Patient medical adhesive remover
Device class
Class I
Regulation number
878.4730
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KOX (Solvent, Adhesive Tape).

Other devices from Safe N Simple LLC

See all devices from Safe N Simple LLC →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)