INVIBIO DEVICE COMPONENT MANUFACTURING, LTD. (IDCM LTD.)

FDA Device Registration & Listing · Thornton Cleveleys Lancashire, GB · Registration 3007791110

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
3007791110
FEI Number
3007791110
Entity Name
INVIBIO DEVICE COMPONENT MANUFACTURING, LTD. (IDCM LTD.)
City/State/Country
Thornton Cleveleys Lancashire, GB
Establishment Address
Hillhouse International, Thornton Cleveleys Lancashire FY5 4QD, GB
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Invibio Device Component Manufacturing, Ltd. (IDCM Ltd.) (Owner Number: 10085461)
Owner / Operator Contact Address
Hillhouse International, Thornton Cleveleys, GB-LAN FY5 4QD, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CoLink PCR Plating System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2022-06-21

Official Correspondent

Caroline Prisk

US Agent Details

Michael Wallick Business: Invibio Email: mwallick@invibio.com Phone: (484) 3426051

Related Public Records

Same Entity

Invibio Device Component Manufacturing, Ltd. (IDCM Ltd.)
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
K042598 Zimmer, Inc. PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES 2004-10-29
K190842 Jiangsu Trauhui Medical Instrument Co., Ltd. Comus Locking Plate systems 2020-02-03
K130510 Arthrex, Inc. ARTHREX COMPRESSION PLATES 2013-09-25
K202803 Newclip Technics Activmotion S DTO 2021-12-16

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2022 Flower Orthopedics Corporation 2
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007791110. Last updated year: 2026. Please use registration number 3007791110 when referencing this establishment in official correspondence.
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