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Florida Probe

FDA UDI

Class I (US FDA UDI)

by Florida Probe Corp.

Identity

Trade Name
Florida Probe FDA UDI
Generic Name
Dental surgical probe, single-use FDA UDI
Device Name
Florida Probe Dolphin Disposable Handpiece. Single use periodontal probe with a titanium probe tip. FDA UDI
Model / Reference
G4 FDA UDI
Description
Florida Probe Dolphin Disposable Handpiece. Single use periodontal probe with a titanium probe tip. FDA UDI

Identifiers

Primary DI / UDI-DI
00856364008103 FDA UDI
FDA Product Code
EIX FDA UDI
GMDN Term
Dental surgical probe, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental surgical probe, single-use

Florida Probe by Florida Probe Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical probe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Florida Probe Corp.

Sources (1)

  • FDA UDI 9b1974b4-d5b3-4df5-817a-4abb26492a5e 34 fields · synced Jun 8, 2026