WESLACOVA Troutman

FDA Device Registration & Listing · Troutman, NC, US · Registration 3025663209

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
3025663209
FEI Number
3025663209
Entity Name
WESLACOVA Troutman
City/State/Country
Troutman, NC, US
Establishment Address
143 Iredell Avenue, Troutman, NC 28166, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Weslacova Corp (Owner Number: 10079247)
Owner / Operator Contact Address
2070 River Road, Liberty Grove Church Road, North Wilkesboro, NC 28659, 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
LRP Tray, Surgical General, Plastic Surgery Class 1 878.4800 2022-01-03
ILI Sling, Arm Physical Medicine Class 1 890.3640 2021-06-16

Official Correspondent

Robert Mauney

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Weslacova Corp
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3009600453 WESLACOVA North Wilkesboro, NC, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K881095 CooperVision, Inc. KOI(TM) INSTRUMENT TRAYS 1988-04-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0036-2010 Alphatec Spine, Inc. 1
ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025663209. Last updated year: 2026. Please use registration number 3025663209 when referencing this establishment in official correspondence.
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