← Back to catalogue

Clarity

FDA UDI

Class II (US FDA UDI)

by Z Microsystems, Inc.

Identity

Trade Name
Clarity FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
The Clarity System delivers significant capabilities to improve the contrast, color, saturation and sharpness of surgical video. FDA UDI
Model / Reference
ZMED-2XYAC-019 FDA UDI
Description
The Clarity System delivers significant capabilities to improve the contrast, color, saturation and sharpness of surgical video. FDA UDI

Identifiers

Catalog Number
ZMED-2XYAC-019 FDA UDI
Primary DI / UDI-DI
00869958000117 FDA UDI
510(k) Number
K130929 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Endoscopic video image processing unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic video image processing unit

Clarity by Z Microsystems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing unit.

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

Sources (1)

  • FDA UDI d1802849-209d-4247-84a6-fdc62a163c3a 36 fields · synced Jun 1, 2026