Sharps Compliance, Inc.

FDA Device Registration & Listing · Houston, TX, US · Registration 3007508552

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
3007508552
FEI Number
3007508552
Entity Name
Sharps Compliance, Inc.
City/State/Country
Houston, TX, US
Establishment Address
2730 Reed Rd., Suite 200, Houston, TX 77051, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
SHARPS COMPLIANCE, INC. (Owner Number: 9041198)
Owner / Operator Contact Address
9220 KIRBY DR., SUITE 500, --, Houston, TX 77054, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

IV POLES PITCH-IT Transport Tube 1.5-Quart Sharps Collection Container 1-Quart Sharps Collection Container

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FOX Stand, Infusion General Hospital Class 1 880.6990 2000-04-27
MMK Container, Sharps General Hospital Class 2 880.5570 2009-01-06
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2005-11-08

Official Correspondent

Curtis Knisley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SHARPS COMPLIANCE, 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
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007508552. Last updated year: 2026. Please use registration number 3007508552 when referencing this establishment in official correspondence.
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