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Retainer - Natural SRI-0202223

by Sprintray, Inc.

Retainer - Natural SRI-0202223 is a Class I device made by Sprintray, Inc., listed in FDA GUDID since 29 Jul 2026 (UDI-DI 00850070544849), 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 Number00850070544849 UDI-DI Date29 Jul 2026ListedStatusListed 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  • Withdrawn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
Retainer - Natural
Generic name
Dental appliance fabrication material, resin
Model / reference
SRI-0202223
Primary DI / UDI-DI
00850070544849
FDA product code
DYJ
GMDN term
Dental appliance fabrication material, resin
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Other devices from Sprintray, Inc.

See all devices from Sprintray, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)