Exmoor Plastics Limited

FDA Device Registration & Listing · Chorley Lancashire, GB · Registration 3002806953

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
3002806953
FEI Number
3002806953
Entity Name
Exmoor Plastics Limited
City/State/Country
Chorley Lancashire, GB
Establishment Address
1 Western Avenue, Buckshaw Village, Matrix Park, Chorley Lancashire PR7 7NB, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Exmoor Plastics Ltd. (Owner Number: 10025024)
Owner / Operator Contact Address
Matrix Park, Buckshaw Village, Chorley, GB-LAN PR7 7NB, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Single Use Myringotomy Kits Titanium ventilation tube Suction Clearance Kit Exmoor Single Use Myringotome Exmoor Silicone Rubber Sheet Exmoor Aural Specula Bel-Air ventilation tube

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JYM Inserter, Myringotomy Tube Ear, Nose, Throat Class 1 874.4420 2008-03-10
ETD Tube, Tympanostomy Ear, Nose, Throat Class 2 874.3880 2019-08-09
LRC Instrument, Ent Manual Surgical Ear, Nose, Throat Class 1 874.4420 2008-03-10
KHJ Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material) Ear, Nose, Throat Class 2 874.3620 2008-03-10
EPY Speculum, Ent General, Plastic Surgery Class 1 878.1800 2008-03-10
ETD Tube, Tympanostomy Ear, Nose, Throat Class 2 874.3880 2019-08-09

Official Correspondent

Anna Gabbott

US Agent Details

Tom Thorelli Business: Thorelli & Associates Email: office@thorelli.com Phone: (312) 3570300

Related Public Records

Same Entity

Exmoor Plastics 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
K143738 Intuit Medical Products, LLC DSS Sinusplasty Balloon Catheter 2015-08-27
K080022 Vascular Solutions, Inc. GEL-SPONGE ENT, ABSORBABLE GELATIN SPONGE, USP 2008-12-09
K834189 Imm Enterprises , Ltd. JAKOBI SURG. INSTRUMENTS #7 44/47 1984-03-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002806953. Last updated year: 2026. Please use registration number 3002806953 when referencing this establishment in official correspondence.
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