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Hu-Friedy TN5482

by Hu-Friedy Mfg Co., LLC

Hu-Friedy TN5482 is a Class I device made by Hu-Friedy Mfg Co., LLC, listed in FDA GUDID since 12 Nov 2020 (UDI-DI 10889950098995), 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 Number10889950098995 UDI-DI Date12 Nov 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  • Withdrawn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
Hu-Friedy
Generic name
Dental restoration carver, resin
Model / Ref / Catalog
TN5482
Primary DI / UDI-DI
10889950098995
FDA product code
EIY
GMDN term
Dental restoration carver, resin
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental restoration carver, resin

Other devices from Hu-Friedy Mfg Co., LLC

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)