Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007086345

FEI Number

3007086345

Entity Name

Sunlight Medical, Inc.

City/State/Country

Jacksonville, FL, US

Establishment Address

5570 Florida Mining Blvd S Ste 603, Jacksonville, FL 32257, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Sunlight Medical, Inc. (Owner Number: 10025905)

Owner / Operator Contact Address

5570 Florida Mining BLVD S., Suite 603, Jacksonville, FL 32257, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K092554

PMA Number

N/A

All Registered Proprietary Names

Blastomere biopsy pipette Polar body biopsy pipette

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQH	Microtools, Assisted Reproduction (Pipettes)	Obstetrics/Gynecology	Class 2	884.6130	2010-05-03

Official Correspondent

Dunsong Yang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sunlight Medical, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007086345. Last updated year: 2026. Please use registration number 3007086345 when referencing this establishment in official correspondence.