Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006315109

FEI Number

3006315109

Entity Name

SPINALIGHT INC

City/State/Country

St Petersburg, FL, US

Establishment Address

2201 62ND AVENUE NORTH, St Petersburg, FL 33702, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Spinalight Inc (Owner Number: 9102583)

Owner / Operator Contact Address

2201 62nd Avenue North, Saint Petersburg, FL 33702, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K172536

PMA Number

N/A

All Registered Proprietary Names

Atlas Percussion Adjusting Instrument

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXM	Manipulator, Plunger-Like Joint	Unknown	Class U	N/A	2022-10-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Spinalight 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 3006315109. Last updated year: 2026. Please use registration number 3006315109 when referencing this establishment in official correspondence.