Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2529776

FEI Number

1000121196

Entity Name

PEPPER MEDICAL, INC.

City/State/Country

West Chester, PA, US

Establishment Address

600 W Strasburg Rd, West Chester, PA 19382, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device

Owner / Operator

PEPPER MEDICAL, INC. (Owner Number: 9006041)

Owner / Operator Contact Address

600 W Strasburg Road, West Chester, PA 19382, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PEPPER MEDICAL FOLEY CATHETER HOLDE LEGBAND HEPA Filter Foley-Patch Foley Tube Holder Foley Loc Tube Tie TRACH TUBE NECKBAND (VARIOUS SIZES) Closed Suction Catheter Bacterial Viral Filter nasal tubing set - various sizes AVALON AIRE HEADSTRAP PEPPER ABDOMINAL BINDER

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EYJ	Holder, Ureteral Catheter	Gastroenterology, Urology	Class 1	876.5130	2002-08-06
CAH	Filter, Bacterial, Breathing-Circuit	Anesthesiology	Class 2	868.5260	2014-01-10
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2012-02-13
JAY	Support, Breathing Tube	Anesthesiology	Class 1	868.5280	2001-11-02
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2025-05-22
CAH	Filter, Bacterial, Breathing-Circuit	Anesthesiology	Class 2	868.5260	2022-04-06
BZO	Set, Tubing And Support, Ventilator (W Harness)	Anesthesiology	Class 1	868.5975	2014-02-26
BTK	Strap, Head, Gas Mask	Anesthesiology	Class 1	868.5560	2006-03-13
FSD	Binder, Abdominal	General Hospital	Class 1	880.5160	2006-03-13

Official Correspondent

MICHELE SCHUSTER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PEPPER MEDICAL, 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
K962045	Mallinckrodt Medical	ANESTHESIA BREATHING CIRCUIT/ANESTHESIA BREATHING KIT	1996-11-26
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-0031-2026	Percussionaire Corporation	1	Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

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3033796310	TAICANG YIGAO MEDICAL TECHNOLOGY CO.,LTD	Taicang Jiangsu, CN
3013576717	CATHETRIX LTD	Yehud Monosun Tel Aviv, IL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2529776. Last updated year: 2026. Please use registration number 2529776 when referencing this establishment in official correspondence.