D.T. DAVIS ENTERPRISES LTD.

FDA Device Registration & Listing · Allentown, PA, US · Registration 2531468

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
2531468
FEI Number
3001600982
Entity Name
D.T. DAVIS ENTERPRISES LTD.
City/State/Country
Allentown, PA, US
Establishment Address
4482 Innovation Way, Allentown, PA 18109, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
D.T. DAVIS ENTERPRISES LTD. T/A HoverTech International (Owner Number: 9033042)
Owner / Operator Contact Address
4482 Innovation Way, --, Allentown, PA 18109, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Q2Roller SitASSIST Safety-Slide HoverMatt PROS HoverJack HoverMatt PROS Sling AirWedge HoverCover Fitted Disposable Sheet HoverCover Three-QTR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2009-02-11
FNG Lift, Patient, Ac-Powered General Hospital Class 2 880.5500 2008-01-08
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2024-04-11
FNG Lift, Patient, Ac-Powered General Hospital Class 2 880.5500 2013-01-07
KME Bedding, Disposable, Medical General Hospital Class 1 880.6060 2017-01-16

Official Correspondent

Dennis Lutz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

D.T. DAVIS ENTERPRISES LTD. T/A HoverTech International
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
K912769 Century Manufacturing Co. PATIENT LIFT AND TRANSPORT 1991-10-02

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 2531468. Last updated year: 2026. Please use registration number 2531468 when referencing this establishment in official correspondence.
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