Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1123029

FEI Number

1000123280

Entity Name

KERMA MEDICAL PRODUCTS, INC.

City/State/Country

Suffolk, VA, US

Establishment Address

215 Suburban Dr, Suffolk, VA 23434, US

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device

Owner / Operator

Kerma Medical Products, Inc. (Owner Number: 9004008)

Owner / Operator Contact Address

215 Suburban Drive, Suffolk, VA 23434, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

FMB

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISR	Band Or Belt, Pelvic Support	Physical Medicine	Class 1	890.3025	2009-02-09

Official Correspondent

Jeffery Hurley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kerma Medical Products, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1123029. Last updated year: 2026. Please use registration number 1123029 when referencing this establishment in official correspondence.