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Tissue-Tek® 6508

by Sakura Finetek USA, Inc

Tissue-Tek 6508 is a barcode reader (FDA Class I; FDA product code KIM, Device for Sealing Microsections) made by Sakura Finetek USA, Inc, listed in FDA GUDID since 17 Mar 2020 (UDI-DI 00615233080837), registry data as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00615233080837 UDI-DI Date17 Mar 2020ListedStatusListed 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  • Withdrawn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
Tissue-Tek®
Generic name
Barcode reader
Model / Ref / Catalog
6508
Primary DI / UDI-DI
00615233080837
FDA product code
KIM
GMDN term
Barcode reader
Device class
Class I
Regulation number
864.3400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Barcode reader

Similar devices

Other devices filed under FDA product code KIM (DEVICE FOR SEALING MICROSECTIONS).

Other devices from Sakura Finetek USA, Inc

See all devices from Sakura Finetek USA, Inc →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)