Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008034554

FEI Number

3008034554

Entity Name

XL PRECISION TECHNOLOGIES LTD

City/State/Country

Stockton on Tees Stockton-on-Tees, GB

Establishment Address

79 Sadler Forster Way, Stockton on Tees Stockton-on-Tees TS17 9JY, GB

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

XL Precision Technologies Ltd (Owner Number: 10060853)

Owner / Operator Contact Address

79 Sadler Forster Way, Stockton on Tees, GB-STT TS17 9JY, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Hydrodam Re-usable Obturator Shaft 5mm Hydrodam Re-usable Obturator Shaft 8.5mm Hydrodam Re-usable Obturator Handle Hydrodam Re-usable Obturator Shaft 7mm

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GEA	Cannula, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2019-07-03

Official Correspondent

Laura Robinson

US Agent Details

Kavetha Ram Business: Spectra Medical Devices, LLC Email: regulatory@spectramedical.com Phone: (978) 6570889

Related Public Records

Same Entity

XL Precision Technologies 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
K863293	Lifestream Int'L, Inc.	DISPOSABLE SUCTION CANNULA NO. 902008-000	1986-09-09

Similar Registrations

Registration Number	Establishment Name	Location
3023138850	AQ THERAPEUTICS, INC.	Irvine, CA, US
1526439	DEPUY SPINE, INC.	RAYNHAM, MA, US
1058584	Sterigenics US LLC	Charlotte, NC, US
1221763	ARCH Medical Solutions - Seabrook	SEABROOK, NH, US
8043496	REDA INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008034554. Last updated year: 2026. Please use registration number 3008034554 when referencing this establishment in official correspondence.