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Richline Group, Inc. d/b/a Inverness Version 0

by Richline Group, Inc. 7 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860014537103 UDI-DI Date26 Feb 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Richline Group, Inc. d/b/a Inverness
Generic Name
Ear lobe perforator
Model / Ref / Catalog
Version 0, 000IN2-20000WM
Primary DI / UDI-DI
00860014537103
FDA Product Code
JYS
GMDN Term
Ear lobe perforator
Device Class
Class I
Regulation Number
874.4420
GUDID distribution status
In Commercial Distribution

Other devices from Richline Group, Inc.

See all devices from Richline Group, Inc. →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

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