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Lightning 905004-0003

by Responsive Orthopedics LLC

Lightning 905004-0003 is a Class I device made by Responsive Orthopedics LLC, listed in FDA GUDID since 15 Mar 2022 (UDI-DI 00811714034584), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00811714034584 UDI-DI Date15 Mar 2022ListedStatusListed 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  • Withdrawn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
Lightning
Generic name
Endoscopic surgical probe
Model / reference
905004-0003
Primary DI / UDI-DI
00811714034584
FDA product code
LXH
GMDN term
Endoscopic surgical probe
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscopic surgical probe

Similar devices in this category

Other devices filed under Endoscopic surgical probe.

Other devices from Responsive Orthopedics LLC

See all devices from Responsive Orthopedics LLC →

Properties

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