DESIGN AND SERVICES HUB, LLC

FDA Device Registration & Listing · Hartville, OH, US · Registration 3036503733

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3036503733
FEI Number
3036503733
Entity Name
DESIGN AND SERVICES HUB, LLC
City/State/Country
Hartville, OH, US
Establishment Address
Design And Services Hub, Llc, 224 E Maple St Ste G, Hartville, OH 44632, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Design and Services Hub, LLC (Owner Number: 10092782)
Owner / Operator Contact Address
Design and Services Hub, LLC, 224 E Maple St, Suite G, Hartville, OH 44632, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic Class 2 888.3080 2025-02-18
MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic Class 2 888.3080 2025-02-18

Official Correspondent

Cowan Moore

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Design and Services Hub, LLC
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
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
K223430 Life Spine, Inc. ProLift Micro Expandable Spacer System 2023-05-04
K102293 Globus Medical, Inc. CALIBER SPACER 2011-01-05

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3036503733. Last updated year: 2026. Please use registration number 3036503733 when referencing this establishment in official correspondence.
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