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Apollo APO-FB-ST-LG

by Protech Leaded Eyewear, Inc.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00828039000026 UDI-DI Date7 Apr 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  • Withdrawn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
Apollo
Generic Name
Radiation shielding apron
Model / Ref / Catalog
APO-FB-ST-LG
Primary DI / UDI-DI
00828039000026
FDA Product Code
IWO
GMDN Term
Radiation shielding apron
Device Class
Class I
Regulation Number
892.6500
GUDID distribution status
In Commercial Distribution

Other devices from Protech Leaded Eyewear, 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