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Vitaltec Corporation

Hou Li District Taichung, TW

VITALTEC CORPORATION appears in FDA device records in Hou Li District Taichung, TW. FDA records list 2 510(k) clearances between and , no PMA records 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
0
Recall records
0
Registered establishments
2

510(k) clearance history

FDA records hold 2 510(k) clearances for Vitaltec Corporation between 2010 and 2025. The busiest year on record is 2010, with 1. The most recent is 2025, with 1.

Clearances by year, as a table
510(k) clearance decisions for Vitaltec Corporation, by decision year
YearClearances
20101
20251
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K2429215300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes 6.0-10.0mm; 5310600-5311000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, Fenestrated, sizes 6.0-10.0mm; 5400600-5401000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, sizes 6.0-10.0mm; 5410500-5411000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, Fenestrated, sizes 6.0-10.0mmBTOSubstantially Equivalent
K100480ROTA-TRACH TRACHEOSTOMY TUBE MODEL ROTA-TRACHBTOSubstantially Equivalent

Registered establishments

FDA registered establishments for Vitaltec Corporation, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30038519063003851906VITALTEC CORPORATIONNo.12, Lane 4-30, Chyuan Zhou Rd.,, Hou Li District Taichung 42142 TW2026
30402798323040279832VITALTEC CORPORATIONNo. 12, Lane 4-30, Chyuan-Zhou Rd., Hou-Li Dist.,, Taichung 42142 TW2026

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