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Algiamed Technologies USA Inc

Lake Mary, FL, US

ALGIAMED TECHNOLOGIES USA INC appears in FDA device records in Lake Mary, FL. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show no recalls 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
0
Registered establishments
1

510(k) clearance history

FDA records hold 1 510(k) clearance for Algiamed Technologies USA Inc in 2026.

Clearances by year, as a table
510(k) clearance decisions for Algiamed Technologies USA Inc, by decision year
YearClearances
20261
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K252712STIMPOD NMS460 Nerve StimulatorGZJSubstantially Equivalent

Registered establishments

FDA registered establishments for Algiamed Technologies USA Inc, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30379672803037967280ALGIAMED TECHNOLOGIES USA INC801 International Pkwy Fl 5, Lake Mary, FL 32746 US2026

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

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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What MDM checks, and what it does not

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