P1 TECHNOLOGIES, INC.

FDA Device Registration & Listing · Cave Spring, VA, US · Registration 1118193

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
1118193
FEI Number
1118193
Entity Name
P1 TECHNOLOGIES, INC.
City/State/Country
Cave Spring, VA, US
Establishment Address
6591 Merriman Rd, Cave Spring, VA 24018, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
P1 TECHNOLOGIES, INC (Owner Number: 1118193)
Owner / Operator Contact Address
6591 MERRIMAN RD, --, Roanoke, VA 24018, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MNR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MNR Ventilatory Effort Recorder Anesthesiology Class 2 868.2375 2023-08-14
IKD Cable, Electrode Physical Medicine Class 2 890.1175 1992-06-22
QPB System, Suction, Lipoplasty For Removal General, Plastic Surgery Class 2 878.5040 2012-12-12
GAA Needle, Aspiration And Injection, Disposable General, Plastic Surgery Class 1 878.4800 2017-02-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

P1 TECHNOLOGIES, 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
K082968 Apneicare, LLC APNEICARE CONNECTION CENTER/INTERNET ANALYSIS 2009-01-02
K781371 Ferris Mfg. Corp. BONE MARROW ASPIRATION KIT 1978-09-20

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2022 NOX MEDICAL Keldnaholt Reykjavik Iceland 2
Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.
Z-0017-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
Z-0018-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle Catalog Number: 4621
Z-0023-2011 Becton Dickinson & Company 1
BD 30G1/2 PrecisionGlide Needle;Catalog/Lot Number: 305106. Needles are intended for use in aspiration and injection of medications.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1118193. Last updated year: 2026. Please use registration number 1118193 when referencing this establishment in official correspondence.
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