PALETTE LIFE SCIENCES

FDA Device Registration & Listing · Santa Barbara, CA, US · Registration 3014909464

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
3014909464
FEI Number
3014909464
Entity Name
PALETTE LIFE SCIENCES
City/State/Country
Santa Barbara, CA, US
Establishment Address
27 East Cota, Suite 402, Santa Barbara, CA 93101, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Palette Life Sciences (Owner Number: 10058510)
Owner / Operator Contact Address
27 East Cota, Suite 402, Santa Barbara, CA 93101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K220641
PMA Number
N/A

All Registered Proprietary Names

Solesta Injectable Gel Barrigel Injectable Gel

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LNM Agent, Bulking, Injectable For Gastro-Urology Use Unknown Class 3 N/A 2018-10-05
OVB Hydrogel Spacer Radiology Class 2 892.5725 2022-05-27

Official Correspondent

Kelsey Krische

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Palette Life Sciences
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0040-06 Boston Scientific Corporation 3
Enteryx Procedure Kit Order No.: M00572600 -US and M00572500 -OUS

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014909464. Last updated year: 2026. Please use registration number 3014909464 when referencing this establishment in official correspondence.
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