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Florida Probe G4

by Florida Probe Corp. 2 variants

Florida Probe G4 is a dental surgical probe (FDA Class I; FDA product code EIX, Probe, Periodontic) made by Florida Probe Corp., listed in FDA GUDID since 8 Aug 2023 (UDI-DI 10856364008100), 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 Number10856364008100 UDI-DI Date8 Aug 2023ListedStatusListed 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  • Withdrawn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
Florida Probe
Generic name
Dental surgical probe, single-use
Model / reference
G4
Primary DI / UDI-DI
10856364008100
FDA product code
EIX
GMDN term
Dental surgical probe, single-use
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental surgical probe, single-use

Similar devices

Other devices filed under FDA product code EIX (Probe, Periodontic).

Other devices from Florida Probe Corp.

See all devices from Florida Probe Corp. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)