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Truepill Inc. 1

by Postmeds, Inc. 2 variants

Truepill Inc. 1 is a Class I device made by Postmeds, Inc., listed in FDA GUDID since 19 May 2022 (UDI-DI 00850032976114), 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 Number00850032976114 UDI-DI Date19 May 2022ListedStatusListed 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  • Withdrawn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
Truepill Inc.
Generic name
Specimen container mailer, non-insulated
Model / reference
1
Primary DI / UDI-DI
00850032976114
FDA product code
NNK
GMDN term
Specimen container mailer, non-insulated
Device class
Class I
Regulation number
864.3250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Specimen container mailer, non-insulatedSpecimen stabilization reagent IVD

Similar devices

Other devices filed under FDA product code NNK (Container, Specimen Mailer And Storage, Non-Sterile).

Other devices from Postmeds, Inc.

Properties

  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (9, all answered No)