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Ceros

FDA UDI

Class II (US FDA UDI)

by HAMILTON THORNE, Inc.

Identity

Trade Name
CEROS FDA UDI
Generic Name
Spermatozoa/semen analyser IVD FDA UDI
Device Name
A modular computerized optical analyzer used for evaluation of sperm samples. It will provide concentration, velocity, morph and motion parameters, which aid the clinician in evaluation of semen quality. FDA UDI
Model / Reference
CEROS FDA UDI
Description
A modular computerized optical analyzer used for evaluation of sperm samples. It will provide concentration, velocity, morph and motion parameters, which aid the clinician in evaluation of semen quality. FDA UDI

Identifiers

Primary DI / UDI-DI
00858604006719 FDA UDI
510(k) Number
K920719 FDA UDI
FDA Product Code
GKL FDA UDI
GMDN Term
Spermatozoa/semen analyser IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5200 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: Spermatozoa/semen analyser IVD

Ceros by HAMILTON THORNE, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spermatozoa/semen analyser IVD.

Cleared under the same submission

K920719 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dc814726-ec94-4d0e-8ac3-ee5e75138971 34 fields · synced May 30, 2026