EHOB Distribution Center W. 21st Street

FDA Device Registration & Listing · Indianapolis, IN, US · Registration 3020225550

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
3020225550
FEI Number
3020225550
Entity Name
EHOB Distribution Center W. 21st Street
City/State/Country
Indianapolis, IN, US
Establishment Address
7901 West 21st Street, Indianapolis, IN 46214, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
EHOB, INC. (Owner Number: 1832066)
Owner / Operator Contact Address
250 NORTH BELMONT AVE., --, Indianapolis, IN 46222, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BAM Air LC Repositioning Sheet BAM Air LC System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2024-08-27

Official Correspondent

James Bui

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EHOB, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3012643605 EHOB (Shanghai) Medical Products Co. Ltd. Pudong Shanghai, CN
3024761165 EHOB(JiaXing) Medical Product Co., LTD. Jiaxing Zhejiang, CN
3018117722 Shanghai EHOB Health Care Products Co., LTD. Shanghai, CN
1832066 EHOB, INC. INDIANAPOLIS, IN, US

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2018 Handicare Usa Inc 1
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018 Handicare AB Maskinvagen 1
Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020225550. Last updated year: 2026. Please use registration number 3020225550 when referencing this establishment in official correspondence.
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