Alcresta Therapeutics, Inc.

FDA Device Registration & Listing · Waltham, MA, US · Registration 3009596666

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
3009596666
FEI Number
3009596666
Entity Name
Alcresta Therapeutics, Inc.
City/State/Country
Waltham, MA, US
Establishment Address
130 Turner Street, Building 3, Suite 200, Waltham, MA 02453, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Alcresta Therapeutics, Inc. (Owner Number: 10050687)
Owner / Operator Contact Address
130 Turner Street, Building 3, Suite 200, Waltham, MA 02453, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K243284
PMA Number
N/A

All Registered Proprietary Names

RELiZORB RELiZORB

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PLQ Enzyme Packed Cartridge Gastroenterology, Urology Class 2 876.5985 2026-02-19
PLQ Enzyme Packed Cartridge Gastroenterology, Urology Class 2 876.5985 2025-11-17

Official Correspondent

Aparajit Panda

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Alcresta Therapeutics, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009596666. Last updated year: 2026. Please use registration number 3009596666 when referencing this establishment in official correspondence.
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