Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010143501

FEI Number

3010143501

Entity Name

FORWARD SCIENCE TECHNOLOGIES LLC

City/State/Country

Houston, TX, US

Establishment Address

10810 Craighead Dr, Houston, TX 77025, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Forward Science LLC (Owner Number: 10043799)

Owner / Operator Contact Address

10810 Craighead Dr, Houston, TX 77025, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

phID SmartFilterID FS Dispenser PerioStom SalivaMAX MucositisRx Orapeutic BioStom OralID FS Dispenser - Stainless

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CEN	Dye-Indicator, Ph (Urinary, Non-Quantitative)	Clinical Chemistry	Class 1	862.1550	2016-03-14
FXQ	Lens, Camera, Surgical	General, Plastic Surgery	Class 1	878.4160	2015-07-30
KCJ	Applicator, Ent	Ear, Nose, Throat	Class 1	874.5220	2023-08-10
MGQ	Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic	Unknown	Class U	N/A	2023-08-08
OLR	Oral Wound Dressing	Unknown	Class U	N/A	2023-08-08
LFD	Saliva, Artificial	Unknown	Class U	N/A	2016-03-14
OLR	Oral Wound Dressing	Unknown	Class U	N/A	2019-12-11
NXV	Diagnostic Light, Soft Tissue Detector	Dental	Class 2	872.6350	2013-03-22
EJB	Handle, Instrument, Dental	Dental	Class 1	872.4565	2024-08-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Forward Science LLC

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
K954741	Derma Sciences, Inc.	DERMAGRAN WENT DRESSING (DEXTROSE-SALINE)	1995-11-01

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0001-05	DeRoyal Wound Care	U	Aquasorb Border, Hydrogel Wound Dressing with Polyurethane Film Border, 25 individual packets per case, Catalog # 46-511, 2.5' x 2.5', labeled in part *SterileManufacturer: DeRoyal 200 Debusk Lane Powell, TN 37849 USA**

Similar Registrations

Registration Number	Establishment Name	Location
1649661	GERMAINE LABORATORIES, INC.	SAN ANTONIO, TX, US
3002637618	Siemens Healthcare Diagnostics Inc	East Walpole, MA, US
3008517993	ZHEJIANG ORIENT GENE BIOTECH	Huzhou Zhejiang, CN
1417592	MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, US
9615507	ACON BIOTECH (HANGZHOU) CO., LTD.	HANGZHOU Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010143501. Last updated year: 2026. Please use registration number 3010143501 when referencing this establishment in official correspondence.