Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031743608

FEI Number

3031743608

Entity Name

QUALITY RECOVERY

City/State/Country

Evans City, PA, US

Establishment Address

1324 Mars Evans City Rd., Suite 2L, Evans City, PA 16033, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Quality Recovery (Owner Number: 10091142)

Owner / Operator Contact Address

1324 Mars Evans City Rd., Suite 2L, Evans City, PA 16033, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Quality Recovery Kit Quality Recovery Tape and Bandage Adhesive

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MCY	Wound Dressing Kit	General Hospital	Class 2	880.5075	2024-07-11
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2024-07-11

Official Correspondent

Adam Griggs

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Quality Recovery

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

Similar Registrations

Registration Number	Establishment Name	Location
3015967359	Stryker Instruments	Portage, MI, US
2433012	BUSSE HOSPITAL DISPOSABLES	HAUPPAUGE, NY, US
9616088	Convertors de Mexico S. de R.L. de C.V	CD.JUAREZ Chihuahua, MX
3016758972	ANJI SPENQ INDUSTRIAL CO., LTD.	Huzhou Zhejiang, CN
3004122598	PRODUCTOS MEDLINE S.A. DE C.V.	NUEVO LAREDO Tamaulipas, MX

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031743608. Last updated year: 2026. Please use registration number 3031743608 when referencing this establishment in official correspondence.