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Vesta

FDA UDI

Class II (US FDA UDI)

by Stratus Medical LLC

Identity

Trade Name
Vesta FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe cannula, single-use FDA UDI
Device Name
Vesta RF Cannula FDA UDI
Model / Reference
NLT-100-18-10-BB FDA UDI
Description
Vesta RF Cannula FDA UDI

Identifiers

Primary DI / UDI-DI
00850040767049 FDA UDI
510(k) Number
K190259 FDA UDI
FDA Product Code
GXI FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4725 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Percutaneous radio-frequency ablation probe cannula, single-use

Vesta by Stratus Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation probe cannula, single-use.

Cleared under the same submission

K190259 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stratus Medical LLC

Sources (1)

  • FDA UDI c118c409-df55-4936-a226-0821fb1e58d2 34 fields · synced Jun 1, 2026