FDA Device Intelligence
Home › Revelle Aesthetics, Inc. › Alite

Alite

Revelle Aesthetics, Inc. · Model AVE003 · UDI-DI 00850036790020

FTD Prescription
10
510(k) clearances
1,240
Adverse events (2 deaths)
49
Recalls
59
Facilities

Description

Alite is a single-use disposable fiber-optic surgical lamp intended to provide visible illumination of the patient’s subcutaneous space as a visual aid in the delivery of solutions. Alite is only compatible with the 3.5-inch, 18 gauge needles specified in the Instructions for Use. The device consists of a Handle that houses the light delivery system and fluid pathway, the Light Fiber, male and female luer connectors, and a Pull Tab.

Recalls

DateFirmReason
2024-06-04Baxter Healthcare CorporationBaxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products l
2024-06-04Baxter Healthcare CorporationBaxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products l
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2019-05-28Maquet Cardiovascular Us Sales, LlcPotential that the coating of the light head forks on the VOLISTA Surgical Lights may crack, posing the risk of particles falling into the surgical field during surgery that may re
2019-05-28Maquet Cardiovascular Us Sales, LlcPotential that the coating of the light head forks on the VOLISTA Surgical Lights may crack, posing the risk of particles falling into the surgical field during surgery that may re

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.