Data / Medical devices / United States / Tiger Aesthetics Medical-SD

Tiger Aesthetics Medical-SD: FDA-registered device maker in San Diego, CA, United States, 3 510(k) clearances and 1 PMA approval

Name: Tiger Aesthetics Medical-SD FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Tiger Aesthetics Medical-SD is registered with the FDA (registration 3003707320) in San Diego, CA, United States. It lists 5 device types. The FDA files 3 510(k) clearances and 1 PMA approval under its listings, the newest dated August 18, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3003707320
Address: 5870 Pacific Center Blvd, San Diego, CA, United States, 92121
Owner or operator: Tiger Aesthetics Medical (10090709)
Roles: Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer
First device listed: January 24, 2025
Registered through: 2026
Brand names listed: Alite, Aveli

Devices it lists

Device	Product code	Class	Role	Source
Dissector, Surgical, General & Plastic Surgery	GDI	1	Complaint file establishment, Manufacturer, Specification developer	accessdata.fda.gov
Implant, Dermal, For Aesthetic Use	LMH	3	Manufacturer	accessdata.fda.gov
Lamp, Surgical	FTD	2	Complaint file establishment, Manufacturer, Specification developer	accessdata.fda.gov
Platelet And Plasma Separator For Bone Graft Handling	ORG	2	Complaint file establishment, Repackager or relabeler, Specification developer	accessdata.fda.gov
Powered Surgical Instrument For Improvement In The Appearance Of Cellulite	OUP	2	Complaint file establishment, Manufacturer, Specification developer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
August 18, 2023	K232153	Avéli	OUP	Substantially Equivalent	Revelle Aesthetics, Inc.	accessdata.fda.gov
August 5, 2022	K221336	Avéli	OUP	Substantially Equivalent	Revelle Aesthetics, Inc.	accessdata.fda.gov
October 22, 2021	K212399	Aveli	OUP	Substantially Equivalent	Nc8, Inc.	accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Approved	PMA number	Device	Product code	Supplements	Latest decision	Source
October 27, 2006	P020012	ARTEFILL, BELLAFILL PMMA COLLAGEN PERMANENT DERMAL FILLER	LMH	43	August 7, 2026	accessdata.fda.gov

Compare with other makers

Updated August 7, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.