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Dxtx Medical Inc.

Pittsburgh, PA, US

DXTX MEDICAL INC. appears in FDA device records in Pittsburgh, PA. FDA records list 2 510(k) clearances between and , 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
2
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 2 510(k) clearances for Dxtx Medical Inc. between 2023 and 2025. The busiest year on record is 2023, with 1. The most recent is 2025, with 1.

Clearances by year, as a table
510(k) clearance decisions for Dxtx Medical Inc., by decision year
YearClearances
20231
20251
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K243428e2CoilTM Imaging System for the Siemens MAGNETOM 3.0T MRI Systems with Tim 4G ConnectorMOSSubstantially Equivalent
K223249Pro-Tx Endorectal Balloon (PROT-25)PCTSubstantially Equivalent

Registered establishments

FDA registered establishments for Dxtx Medical Inc., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30154317113015431711DXTX MEDICAL INC.639 Alpha Drive, Pittsburgh, PA 15238 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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Data as of , FDA export datePage updated Source: openFDA, public domain