Oricare Inc.

FDA Device Registration & Listing · Quakertown, PA, US · Registration 3009129579

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
3009129579
FEI Number
3009129579
Entity Name
Oricare Inc.
City/State/Country
Quakertown, PA, US
Establishment Address
1900 Am Dr, Quakertown, PA 18951, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Oricare Inc. (Owner Number: 10036506)
Owner / Operator Contact Address
1900 AM Drive, Quakertown, PA 18951, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

A9800 Anesthesia Workstation T3600 Surgical Table LuvRes F2NV LuvRes F1NV L2700 Surgical Lights

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BSZ Gas-Machine, Anesthesia Anesthesiology Class 2 868.5160 2014-06-06
GDC Table, Operating-Room, Electrical General, Plastic Surgery Class 1 878.4960 2011-05-12
BYG Mask, Oxygen Anesthesiology Class 1 868.5580 2025-12-14
FSY Light, Surgical, Ceiling Mounted General, Plastic Surgery Class 2 878.4580 2013-01-03

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Oricare 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
K252746 Drägerwerk AG Co. Kgaa Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL) 2026-05-21
K780666 Castle Co. DAYSTAR SELECTRA & SELECTRA/ORBITER 1978-04-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-2011 GE Healthcare, LLC 2
GE Datex-Ohmeda Aisys Anesthesia System, manufactured by GE Healthcare, P.O. Box 900, FIN-00031 GE, Finland
Z-0008-2014 Draeger Medical, Inc. 2
Draeger Fabius GS Premium, Fabius OS, Fabius Tiro, Fabius Tiro D-M Product Usage: used to administer anesthesia and ventilation to patients during surgical procedures.
Z-0009-2011 GE Healthcare, LLC 2
GE Datex-Ohmeda Avance Anesthesia System, manufactured by GE Healthcare, P.O. Box 900, FIN-00031 GE, Finland
Z-0009-2014 GE Healthcare, LLC 2
GE Healthcare, Aisys, Amingo, Avance, and Avance CS2. Intended for volume or pressure control ventilation.
Z-0010-2011 GE Healthcare, LLC 2
GE Datex-Ohmeda Amingo Anesthesia System, manufactured by GE Healthcare, P.O. Box 900, FIN-00031 GE, Finland

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2112667 Datex-Ohmeda, Inc. MADISON, WI, US
3003589956 Flextronics Manufacturing (Singapore) Pte Ltd SINGAPORE South East, SG
3005803793 THORNHILL RESEARCH INC. TORONTO Ontario, CA
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009129579. Last updated year: 2026. Please use registration number 3009129579 when referencing this establishment in official correspondence.
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