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

Allentown, PA, US

D.T. DAVIS ENTERPRISES LTD. appears in FDA device records in Allentown, PA. 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 D.T. Davis Enterprises Ltd. in 2004.

Clearances by year, as a table
510(k) clearance decisions for D.T. Davis Enterprises Ltd., by decision year
YearClearances
20041
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K041503HOVERJACK AIR PATIENT LIFT DEVICEFNGSubstantially Equivalent

Registered establishments

FDA registered establishments for D.T. Davis Enterprises Ltd., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
25314683001600982D.T. DAVIS ENTERPRISES LTD.4482 Innovation Way, Allentown, PA 18109 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-0084-06HoverMatt Patient Transfer Solution/Air Transfer MattressInstructions for use are not adhering to the productTerminated

Verification record

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