510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Guilin Kevin Peter Technology Co., Ltd.

Guilin Guangxi, CN

GUILIN KEVIN PETER TECHNOLOGY CO., LTD. appears in FDA device records in Guilin Guangxi, CN. 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 Guilin Kevin Peter Technology Co., Ltd. in 2026.

Clearances by year, as a table
510(k) clearance decisions for Guilin Kevin Peter Technology Co., Ltd., by decision year
YearClearances
20261
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K261415Injectable Root Canal Sealer (KP-Root SP)KIFSubstantially Equivalent

Registered establishments

FDA registered establishments for Guilin Kevin Peter Technology Co., Ltd., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30238167203023816720GUILIN KEVIN PETER TECHNOLOGY CO., LTD.North side of Linsu Rd, Lingui Town, Lingui Dist., Guilin, Guilin Guangxi 541100 CN2026and 6 more, listed in full below

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

There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.

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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