Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2950160

FEI Number

1000123971

Entity Name

WRIGHT ENGINEERED PLASTICS, INC.

City/State/Country

Santa Rosa, CA, US

Establishment Address

3681 N Laughlin Rd, Santa Rosa, CA 95403, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Repack or Relabel Medical Device

Owner / Operator

WRIGHT ENGINEERED PLASTICS, INC. (Owner Number: 9002508)

Owner / Operator Contact Address

3681 North Laughlin Road, --, Santa Rosa, CA 95403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

InTrack Jaw Inserts Encore, Activities Luna XD Graft Injector DXC - InTrack Inserts Enclose Novaclips & Greyhound Spring Clips Asteme Encore Revision Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2014-07-03
ORY	Tongue Suspension System	Dental	Class 2	872.5570	2020-10-15
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2020-04-23
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2017-10-27
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2014-07-03
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2014-07-03
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2006-02-06
HXC	Wrench	Orthopedic	Class 1	888.4540	2019-07-26

Official Correspondent

Tom Orr

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WRIGHT ENGINEERED PLASTICS, INC.

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
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
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.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011	Depuy Orthopaedics, Inc.	1	Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

Registration Number	Establishment Name	Location
1531062	E-BEAM SERVICES, INC.	LEBANON, OH, US
9680515	TONTARRA MEDIZINTECHNIK GMBH	WURMLINGEN Baden-Wurttemberg, DE
1055236	DEROYAL INDUSTRIES, INC.	NEW TAZEWELL, TN, US
3005809810	Jarit GmbH	Rietheim-Weilheim Baden-Wurttemberg, DE
2030624	Isomedix Operations, Inc.	Temecula, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2950160. Last updated year: 2026. Please use registration number 2950160 when referencing this establishment in official correspondence.