Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010760216

FEI Number

3010760216

Entity Name

TRICE MEDICAL

City/State/Country

Malvern, PA, US

Establishment Address

40 General Warren Blvd, Suite 100, Malvern, PA 19355, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Trice Medical (Owner Number: 10046410)

Owner / Operator Contact Address

40 General Warren Blvd, Suite 100, Malvern, PA 19355, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SegWAY Instrument Case mi-probe mi-eye SegWay Disposable ECTR Kit Advansor Trigger Finger Release System SegWAY Guides C-MOR Visualization Device mi-eye 3 mi-eye 2 mi-tablet 2 SegWAY Instruments

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2019-11-20
HXB	Probe	Orthopedic	Class 1	888.4540	2018-03-16
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2014-09-23
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	2017-11-06
FZX	Guide, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2019-11-20
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2014-03-19
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2021-12-15
HRX	Arthroscope	Orthopedic	Class 2	888.1100	2017-05-04
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2019-11-20

Official Correspondent

David Vancelette

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Trice Medical

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
K081051	Spine View, Inc.	SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS), SPINEVU MINISCOPE	2008-08-07
K820777	The Anspach Effort, Inc.	MINI-MICRO ARTHROSCOPIC SCAPEL	1982-05-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
Z-0041-05	Linvatec Corp.	2	Ultra Power Burs, Sterile, Single-Use.
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.

Similar Registrations

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3008886285	Flextronics International Kft	Budapest, HU
3012574325	HAKAMA AG	Baettwil Solothurn, CH
3001397320	ROECHLING MEDICAL ROCHESTER L.P.	Rochester, NY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010760216. Last updated year: 2026. Please use registration number 3010760216 when referencing this establishment in official correspondence.