Skip to content

Europa Solo-Pack SEEFL113CS

by G&H Wire Company, Inc.

Europa Solo-Pack SEEFL113CS is a Class I device made by G&H Wire Company, Inc., listed in FDA GUDID since 26 Mar 2025 (UDI-DI 10190886025338), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10190886025338 UDI-DI Date26 Mar 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  • Withdrawn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

Trade name
Europa Solo-Pack
Generic name
Orthodontic archwire
Model / reference
SEEFL113CS
Primary DI / UDI-DI
10190886025338
FDA product code
DZC
GMDN term
Orthodontic archwire
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — .013 Inch

Related devices

Category: Orthodontic archwire

Other devices from G&H Wire Company, Inc.

See all devices from G&H Wire Company, Inc. →

Properties

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