510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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NEUROLIEF Inc.

Netanya Central, IL

NEUROLIEF Inc. appears in FDA device records in Netanya Central, IL. FDA records list 2 510(k) clearances between and , one PMA record and 2 registered establishments. 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
2
PMA records
1
Recall records
0
Registered establishments
2

510(k) clearance history

FDA records hold 2 510(k) clearances for NEUROLIEF Inc. in 2021.

Clearances by year, as a table
510(k) clearance decisions for NEUROLIEF Inc., by decision year
YearClearances
20212
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K212106RelivionPCCSubstantially Equivalent
K203419RelivionPCCSubstantially Equivalent

Registered establishments

FDA registered establishments for NEUROLIEF Inc., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30195511443019551144NEUROLIEF Inc.10211 W Sample Road #109, Coral Springs, FL 33065 US2026
30150883973015088397NEUROLIEF Ltd.12 Giborei Israel, Netanya Central 4250412 IL2026

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