KAISER MEDICAL INC

FDA Device Registration & Listing · West Grove, PA, US · Registration 3021373887

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3021373887
FEI Number
3021373887
Entity Name
KAISER MEDICAL INC
City/State/Country
West Grove, PA, US
Establishment Address
105 WOODLAND AVE, SUITE #1 #2, West Grove, PA 19390, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KAISER MEDICAL INC (Owner Number: 10083946)
Owner / Operator Contact Address
105 WOODLAND AVE, SUITE #1 #2, West Grove, PA 19390, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

K-ROM KICK OUT D-SPLINTS ELECTRA SHOULDER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BXB Exerciser, Powered Physical Medicine Class 1 890.5380 2025-12-13
ION Exerciser, Non-Measuring Physical Medicine Class 1 890.5370 2025-12-12
KFW Assembly, Shoulder/Elbow/Forearm/Wrist/Hand, Powered Physical Medicine Class 1 890.3420 2022-01-03

Official Correspondent

ROBERT KAISER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KAISER MEDICAL INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021373887. Last updated year: 2026. Please use registration number 3021373887 when referencing this establishment in official correspondence.
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