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Manufacturer profile

Penumbra, Inc.

TaiwanUnited States11 products registeredOct 23, 2009 – Dec 11, 2023
VerifiedTFDA · Taiwan Food and Drug Administration registry
11
Total products
11
Product types
11
Active products
Dec 2023
Latest registration
Company details
Address
One Penumbra Place Alameda, CA 94502, USA;;630 Roseville Parkway, Roseville, CA, 95747, USA
Regulatory footprint
Search Penumbra, Inc. across other regulatory registries
ThailandEuropean UnionColombiaSouth KoreaCanadaEcuador
Recent registrations
Latest 5 products registered by this manufacturer
"Pinabo" Nuno intracranial delivery system
Class 2
Dec 11, 2023
"Pinabo" Pinabo system
Class 2
Jan 06, 2023
"Pinabo" INTICO suction system
Class 2
Dec 14, 2022
“Penumbra” INDIGO Aspiration System CAT RX
Class 2
Nov 01, 2021
“Penumbra” INDIGO Aspiration System
Class 2
Feb 01, 2019
Most popular products
Products with most registrations
"Pinabo" Nuno intracranial delivery system
1 registrations
"Pinabo" Pinabo system
1 registrations
"Pinabo" INTICO suction system
1 registrations
“Penumbra” INDIGO Aspiration System CAT RX
1 registrations
“Penumbra” INDIGO Aspiration System
1 registrations
Authorized representatives
Taiwan authorized representatives for this manufacturer
FRONTIER BIO-MEDICAL INC.
11 products
Recent registered products
Most recent products (showing top 20)
"Pinabo" Nuno intracranial delivery system
Registered: Dec 11, 2023 • Expires: Dec 11, 2028
Risk Class
Class 2
AR
FRONTIER BIO-MEDICAL INC.
"Pinabo" Pinabo system
Registered: Jan 06, 2023 • Expires: Jan 06, 2028
Risk Class
Class 2
AR
FRONTIER BIO-MEDICAL INC.
"Pinabo" INTICO suction system
Registered: Dec 14, 2022 • Expires: Dec 14, 2027
Risk Class
Class 2
AR
FRONTIER BIO-MEDICAL INC.
“Penumbra” INDIGO Aspiration System CAT RX
Registered: Nov 01, 2021 • Expires: Nov 01, 2026
Risk Class
Class 2
Type
MD
AR
FRONTIER BIO-MEDICAL INC.
“Penumbra” INDIGO Aspiration System
Registered: Feb 01, 2019 • Expires: Feb 01, 2029
Risk Class
Class 2
Type
MD
AR
FRONTIER BIO-MEDICAL INC.
“Penumbra” Benchmark Intracranial Access System
Registered: Jul 24, 2018 • Expires: Jul 24, 2028
Risk Class
Class 2
Type
MD
AR
FRONTIER BIO-MEDICAL INC.
“Penumbra” Ruby Coil System
Registered: May 22, 2015 • Expires: May 22, 2025
Risk Class
Class 3
Type
MD
AR
FRONTIER BIO-MEDICAL INC.
“Penumbra” Penumbra System
Registered: Sep 10, 2014 • Expires: Sep 10, 2024
Risk Class
Class 2
Type
MD
AR
FRONTIER BIO-MEDICAL INC.
“Penumbra” Delivery Microcatheters
Registered: May 06, 2014 • Expires: May 06, 2024
Risk Class
Class 2
Type
MD
AR
FRONTIER BIO-MEDICAL INC.
"Pinabo" Newomax system
Registered: May 06, 2013 • Expires: May 06, 2028
Risk Class
Class 2
AR
FRONTIER BIO-MEDICAL INC.
"Pinabo" Newno intracranial introduction system
Registered: Oct 23, 2009 • Expires: Oct 23, 2029
Risk Class
Class 2
AR
FRONTIER BIO-MEDICAL INC.
About this profile

Explore comprehensive manufacturer profile for Penumbra, Inc. based in United States through Pure Global AI's free Taiwan medical device database. This manufacturer has 11 products registered in Taiwan across 11 unique product categories. Their regulatory history spans from Oct 23, 2009 to Dec 11, 2023.

This page provides detailed insights including 5 recent product registrations, 5 most popular products with "Pinabo" Nuno intracranial delivery system having 1 registrations, and 1 authorized representatives including FRONTIER BIO-MEDICAL INC.. Pure Global AI offers free access to Taiwan's medical device database, enabling global MedTech companies to analyze market dynamics and identify opportunities.