Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012172036

FEI Number

3012172036

Entity Name

TASSO INC

City/State/Country

Seattle, WA, US

Establishment Address

400 2nd Ave W, Seattle, WA 98119, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Tasso Inc (Owner Number: 10061412)

Owner / Operator Contact Address

400 2nd Ave W, Seattle, WA 98119, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tasso Mini Tasso+ Tasso-M20 Tasso-M20 Tile-T20 Tasso Mini Standard Kit Tasso+ Standard Kit Tasso-M20 Tasso+

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2022-08-17
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2023-06-12
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2019-10-15
PQD	Blood Specimen Collection Convenience Kit (Excludes Hiv)	Clinical Chemistry	Class 2	862.1675	2021-05-03
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2019-10-15

Official Correspondent

Ben Casavant

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tasso 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
K130132	Medipurpose Pte. , Ltd.	BABYLANCE HEEL INCISION DEVICE	2013-02-11

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0044-2008	Becton Dickinson & Company	2	Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

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3012494290	SANICURE BV	SCHIPHOL Noord-Holland, NL
3007384659	SIMPLE DIAGNOSTICS	Maspeth, NY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012172036. Last updated year: 2026. Please use registration number 3012172036 when referencing this establishment in official correspondence.