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Thunderbolt 909005-0000

by Responsive Orthopedics LLC

Thunderbolt 909005-0000 is a Class I device made by Responsive Orthopedics LLC, listed in FDA GUDID since 15 Mar 2022 (UDI-DI 00811714035000), 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 Number00811714035000 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  • Withdrawn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
Thunderbolt
Generic name
Suture/ligature tightener, reusable
Model / reference
909005-0000
Primary DI / UDI-DI
00811714035000
FDA product code
LXH
GMDN term
Suture/ligature tightener, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Suture/ligature tightener, reusable

Similar devices

Other devices filed under FDA product code LXH (Orthopedic Manual Surgical Instrument).

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)