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Bioprogressive E00818

by Rmo

Bioprogressive E00818 is a Class I device made by Rmo, listed in FDA GUDID since 19 Aug 2024 (UDI-DI 00885797094964), 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 Number00885797094964 UDI-DI Date19 Aug 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  • Withdrawn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
Bioprogressive
Generic name
Orthodontic spring
Model / reference
E00818
Primary DI / UDI-DI
00885797094964
FDA product code
ECO
GMDN term
Orthodontic spring
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic spring

Other devices from Rmo

See all devices from Rmo →

Properties

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