Miller Technical Services

FDA Device Registration & Listing · Plymouth, MI, US · Registration 3006654680

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
3006654680
FEI Number
3006654680
Entity Name
Miller Technical Services
City/State/Country
Plymouth, MI, US
Establishment Address
47801 W Anchor Ct, Plymouth, MI 48170, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Miller Technical Services (Owner Number: 10032618)
Owner / Operator Contact Address
47801 W. Anchor Court, Plymouth, MI 48170, 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
CAC Apparatus, Autotransfusion Anesthesiology Class 2 868.5830 2018-10-12
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2017-08-11
IRT Pad, Heating, Powered Physical Medicine Class 2 890.5740 2024-12-10
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2013-01-30
EBZ Activator, Ultraviolet, For Polymerization Dental Class 2 872.6070 2025-01-05
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2017-08-11
HST Apparatus, Traction, Non-Powered Orthopedic Class 1 888.5850 2021-12-15
FWZ Operating Room Accessories Table Tray General, Plastic Surgery Class 1 878.4950 2020-03-11
HXC Wrench Orthopedic Class 1 888.4540 2020-03-02

Official Correspondent

Patrick Miller

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Miller Technical Services
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
K881350 Stryker Corp. CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM 1988-09-30
K260601 Blue Belt Technologies, Inc. REAL INTELLIGENCE™ CORI™ 2026-03-26
K881862 Thermo Body Wrap Systems, Inc. THERMO-BODY-WRAP SYSTEM 1988-10-13
K243921 Foshan Coxo Medical Instrument Co., Ltd. LED Curing Lights (DB686 HALO) 2025-04-11
K033201 Apoza Enterprise Co., Ltd. LA500 BLUE LIGHT 2003-12-02

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0041-2024 Blue Belt Technologies, Inc 2
Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299

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9680841 SORIN GROUP ITALIA S.R.L MIRANDOLA Modena, IT
1424263 Isomedix Operations, Inc. Libertyville, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006654680. Last updated year: 2026. Please use registration number 3006654680 when referencing this establishment in official correspondence.
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