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Lumithera, Inc.

Fort Worth, TX, US

LUMITHERA, INC. appears in FDA device records in Fort Worth, TX. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show one recall for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
1
PMA records
0
Recall records
1
Registered establishments
1

510(k) clearance history

FDA records hold 1 510(k) clearance for Lumithera, Inc. in 2024.

Clearances by year, as a table
510(k) clearance decisions for Lumithera, Inc., by decision year
YearClearances
20241
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
DEN230083Valeda Light Delivery SystemSDEUnknown

Registered establishments

FDA registered establishments for Lumithera, Inc., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30162320283016232028LUMITHERA, INC.6201 South Fwy, Fort Worth, TX 76134 US2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

Device recall records naming this company, most recent first
RecallProductReasonClassificationInitiatedStatus
Z-2046-2025Brand Name: Valeda Light Delivery System Product Name: Light Based Device for Dry Age Related Macular Degeneration Product Description: Light Based Device for Dry Age Related Macular Degeneration Component: NoU.S. customers were shipped devices that were configured for the European Union and were unable to plug the device in the electrical outlet.Class IIIOpen, Classified

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain