← Back to catalogue

STar™ Drive MA

FDA UDI

Class II (US FDA UDI)

by Fhc, Inc.

Identity

Trade Name
STar™ Drive MA FDA UDI
Generic Name
Neurosurgical micro targeting drive FDA UDI
Device Name
STar(TM) Drive MA, Manual Operation Only FDA UDI
Model / Reference
70-ZD-MA-00216 FDA UDI
Description
STar(TM) Drive MA, Manual Operation Only FDA UDI

Identifiers

Catalog Number
70-ZD-MA FDA UDI
Primary DI / UDI-DI
00873263002162 FDA UDI
510(k) Number
K092562 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Neurosurgical micro targeting drive 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Neurosurgical micro targeting drive

STar™ Drive MA by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical micro targeting drive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fhc, Inc.

Sources (1)

  • FDA UDI be3d5773-ba86-432d-8f55-afc5ccf7ebdf 37 fields · synced Jun 8, 2026