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PressON™ 820294

by Nexus Spine, L.L.C.

PressON™ 820294 is a Class I device made by Nexus Spine, L.L.C., listed in FDA GUDID since 28 Feb 2022 (UDI-DI B6788202940), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB6788202940 UDI-DI Date28 Feb 2022ListedStatusListed 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  • Withdrawn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
PressON™
Generic name
Bone tap, reusable
Model / reference
820294
Primary DI / UDI-DI
B6788202940
FDA product code
LXH
GMDN term
Bone tap, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Width — 7.5 Millimeter

Related devices

Category: Bone tap, reusable

Other devices from Nexus Spine, L.L.C.

See all devices from Nexus Spine, L.L.C. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)