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PDT, Inc. T122 Luxating Instrument (4mm)

by PDT, Inc.

PDT, Inc. T122 Luxating Instrument (4mm) is a periotome (FDA Class I; FDA product code EMO, Knife, Periodontic) made by PDT, Inc., listed in FDA GUDID since 1 Jul 2024 (UDI-DI 00813677022837), 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 Number00813677022837 UDI-DI Date1 Jul 2024ListedStatusListed 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  • Withdrawn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
PDT, Inc.
Generic name
Periotome, reusable
Model / Ref / Catalog
T122 Luxating Instrument (4mm), T122
Primary DI / UDI-DI
00813677022837
FDA product code
EMO
GMDN term
Periotome, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Periotome, reusable

Other devices from PDT, Inc.

See all devices from PDT, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)