P3 MEDICAL LTD

FDA Device Registration & Listing · Bristol Bristol, City of, GB · Registration 3012508471

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
3012508471
FEI Number
3012508471
Entity Name
P3 MEDICAL LTD
City/State/Country
Bristol Bristol, City of, GB
Establishment Address
1 Newbridge Close, Bristol Bristol, City of BS4 4AX, GB
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
P3 Medical Ltd (Owner Number: 10052414)
Owner / Operator Contact Address
1 Newbridge Close, Bristol, GB-BST BS4 4AX, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AIRWAY, OROPHARYNGEAL Robotic Arm Drape Camera Drape Corin Camera drape Drape and Calibration target for use with ActivSight imaging system CoreVista® Monitor Drape. Tablet Drape Versius Equipment Drapes

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAE Airway, Oropharyngeal, Anesthesiology Anesthesiology Class 1 868.5110 2019-07-01
PUI Drape, Surgical, Exempt General, Plastic Surgery Class 2 878.4370 2017-08-17

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: Liberty Management Group Ltd. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

P3 Medical Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2014 King Systems Corp. 1
King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012508471. Last updated year: 2026. Please use registration number 3012508471 when referencing this establishment in official correspondence.
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