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Curble Chair K-Med_Medium_Grey

by ablue.Co., Ltd GUDID

Withdrawn United States

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809395551522 UDI-DIDate14 Oct 2021ListedStatusWithdrawn

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  • Withdrawn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 23 Oct 2026.

Specification

GUDID

Trade Name
Curble Chair
Generic Name
Lumbar spine orthosis
Model / Reference
K-Med_Medium_Grey
Primary DI / UDI-DI
08809395551522
FDA Product Code
IQE
GMDN Term
Lumbar spine orthosis
Device Class
Class I
Regulation Number
890.3490
Commercial Distribution
Not in Commercial Distribution

Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No