Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005977257

FEI Number

3005977257

Entity Name

SPINEFRONTIER, INC. DBA LESspine Innovations

City/State/Country

Burlington, MA, US

Establishment Address

200 Summit Drive, Suite 505, Burlington, MA 01803, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LESspine Innovations (Owner Number: 9094359)

Owner / Operator Contact Address

200 Summit Dr, Suite 505, Burlington, MA 01803, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K142026

PMA Number

N/A

All Registered Proprietary Names

ELID Endoscopic Less Invasive Decompression A-CIFT SoloFuse P-LIFT Dorado E-LIFT S-LIFT T-LIFT Arena-L TILT Arena-C HA

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HAE	Rongeur, Manual	Neurology	Class 2	882.4840	2026-02-04
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2026-02-04
OVE	Intervertebral Fusion Device With Integrated Fixation, Cervical	Orthopedic	Class 2	888.3080	2018-08-13
ODP	Intervertebral Fusion Device With Bone Graft, Cervical	Orthopedic	Class 2	888.3080	2018-08-13
MAX	Intervertebral Fusion Device With Bone Graft, Lumbar	Orthopedic	Class 2	888.3080	2026-01-15
ODP	Intervertebral Fusion Device With Bone Graft, Cervical	Orthopedic	Class 2	888.3080	2015-03-06

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LESspine Innovations

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K081051	Spine View, Inc.	SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS), SPINEVU MINISCOPE	2008-08-07
K820777	The Anspach Effort, Inc.	MINI-MICRO ARTHROSCOPIC SCAPEL	1982-05-12
K142269	Reliance Medical Systems, LLC	Reliance Cervical IBF System	2015-06-09
K122085	Omni Surgical, LP Dba Spine360	STINGRAY CERVICAL CAGE	2012-10-17
K120275	Synthes (Usa), LLC	SYNTHES ACIS/VERTEBRAL SPACER CR	2012-05-25

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0041-05	Linvatec Corp.	2	Ultra Power Burs, Sterile, Single-Use.

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9710524	ULTIMATE MEDICAL PRODUCTS LTD.	SHARJAH Ash Shariqah, AE
1836161	ASPEN SURGICAL PRODUCTS, INC.	Caledonia, MI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005977257. Last updated year: 2026. Please use registration number 3005977257 when referencing this establishment in official correspondence.