Gri Medical & Electronic Technology Co., Ltd.
JIAXING Zhejiang, CN
GRI MEDICAL & ELECTRONIC TECHNOLOGY CO., LTD. appears in FDA device records in JIAXING Zhejiang, CN. FDA records list 4 510(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) clearance history
FDA records hold 4 510(k) clearances for Gri Medical & Electronic Technology Co., Ltd. between 2011 and 2018. The busiest year on record is 2011, with 2. The most recent is 2018, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2011 | 2 |
| 2017 | 1 |
| 2018 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K172835 | GRI-Alleset Veress Needle | HIF | Substantially Equivalent | |
| K172712 | gentleheel Micro-Preemie, gentleheel Preemie, gentleheel Newborn, gentleheel Toddler | FMK | Substantially Equivalent | |
| K111458 | GRI STERILE AND NON-STERILE SURGICAL DRAPES AND SURGICAL EQUIPMENT COVERS | KKX | Substantially Equivalent | |
| K102652 | NON REINFORCED SURGICAL GOWNS, FILM REINFORCED SURGICAL GOWNS, FABRIC REINFORCED SURGICAL GOWNS | FYA | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3004911384 | 3004911384 | GRI MEDICAL & ELECTRONIC TECHNOLOGY CO., LTD. | 1805 HONGGAO ROAD, JIAXING Zhejiang 314031 CN | 2026 | and 63 more, listed in full below |
| 3010807315 | 3010807315 | GRI MEDICAL & ELECTRONIC TECHNOLOGY CO., LTD. | Industrial Zone, Yijiang Town,, Wuhu Anhui 241311 CN | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KGZAccessories, Catheter
- OFQAnesthesia Kit
- OEQAngiography/Angioplasty Kit
- KXFApplicator, Absorbent Tipped, Non-Sterile
- FQMBandage, Elastic
- FNYBasin, Emesis
- KMEBedding, Disposable, Medical
- OESCardiac Catheterization Kit
- OEZCardiovascular Procedure Kit
- JOLCatheter And Tip, Suction
- OFCCatheter Introducer Kit
- DQOCatheter, Intravascular, Diagnostic
- OHMCesarean Section Tray
- HXDClamp
- KPEContainer, I.V.
- KYWContainer, Liquid Medication, Graduated
- FMHContainer, Specimen, Sterile
- FLLContinuous Measurement Thermometer
- FMWCover, Mattress (Medical Purposes)
- OFGCt Biopsy Tray
- HMTDrape, Patient, Ophthalmic
- KKXDrape, Surgical, Antimicrobial
- NADDressing, Wound, Occlusive
- OGREar, Nose, And Throat Surgical Tray
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- FRLFiber, Medical, Absorbent
- GENForceps, General & Plastic Surgery
- NABGauze / Sponge,Nonresorbable For External Use
- GDYGauze/Sponge, Internal, X-Ray Detectable
- LROGeneral Surgery Tray
- FYAGown, Surgical
- OHDGynecological Laparoscopic Kit
- HXKHolder, Needle; Orthopedic
- MDMInstrument, Manual, Surgical, General Use
- HIFInsufflator, Laparoscopic
- MLSLabor And Delivery Kit
- FDELaparoscopy Kit
- FTALight, Surgical, Accessories
- FZZMarker, Skin
- OGSMyringotomy Procedure Kit
- GABNeedle, Suturing, Disposable
- OJGNeurological Tray
- OEANon-Surgical Gown
- OFLPercutaneous Sheath Introducer Kit
- FTNPlastic Surgery And Accessories Kit
- FMQRestraint, Protective
- GDXScalpel, One-Piece
- FPASet, Administration, Intravascular
- LHISet, I.V. Fluid Transfer
- HOYShield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- FMKSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- HOZSponge, Ophthalmic
- CCXSupport, Patient Position
- KYZSyringe, Irrigating (Non Dental)
- FMFSyringe, Piston
- JAASystem, X-Ray, Fluoroscopic, Image-Intensified
- KGXTape And Bandage, Adhesive
- FSMTray, Surgical, Instrument
- GAZTubing, Noninvasive
- NKCTubing/Tubing With Filter, Insufflation, Laparoscopic
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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Data as of , FDA export datePage updated Source: openFDA, public domain
