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Ortho Arch 270-219

by Ortho Arch Company Inc GUDID

Listed (no authorization) FDA GUDID database listing only

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD90927021918 UDI-DIDate29 Sep 2025ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Ortho Arch
Generic Name
Orthodontic power arm
Model / Reference
270-219
Primary DI / UDI-DI
D90927021918
FDA Product Code
DZC
GMDN Term
Orthodontic power arm
Device Class
Class I
Regulation Number
872.5410
Commercial Distribution
In Commercial Distribution

Other devices from Ortho Arch Company Inc

See all devices from Ortho Arch Company Inc →

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No