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PDT, Inc.

by PDT, Inc. 88 variants

PDT, Inc. (T055-3) is a dental mirror (FDA Class I; FDA product code EAX, Mirror, Mouth) made by PDT, Inc., listed in FDA GUDID since 20 Oct 2025 (UDI-DI 00813677025364), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813677025364 UDI-DI Date20 Oct 2025ListedStatusListed 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  • Withdrawn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

Generic name
Dental mirror, reusable
Model / Ref / Catalog
T055-3 Double-Sided PrecisionReflect HD Mirror Three Packket, T055-3
Primary DI / UDI-DI
00813677025364
FDA product code
EAX
GMDN term
Dental mirror, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EAX (Mirror, Mouth).

Other devices from PDT, Inc.

See all devices from PDT, Inc. →

Properties

  • Sterilise before use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)