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microTargeting™ LeadLoc Depth Stop

FDA UDI

Class II (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
microTargeting™ LeadLoc Depth Stop FDA UDI
Generic Name
Neurological stereotactic surgery system FDA UDI
Device Name
LeadLoc Depth Stop FDA UDI
Model / Reference
66-AC-DC-00566 FDA UDI
Description
LeadLoc Depth Stop FDA UDI

Identifiers

Catalog Number
66-AC-DC FDA UDI
Primary DI / UDI-DI
00873263005668 FDA UDI
510(k) Number
K011992 FDA UDI
K092562 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Neurological stereotactic surgery system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 1.6 Millimeter FDA UDI

Category: Neurological stereotactic surgery system

microTargeting™ LeadLoc Depth Stop by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurological stereotactic surgery system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fhc, Inc.

Sources (1)

  • FDA UDI f25bb3c6-04a7-4ded-8ed4-9d43aa97024f 38 fields · synced May 31, 2026