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BK MEDITECH CO., LTD.

US

Last updated May 23, 2026

What BK MEDITECH CO., LTD. makes

BK Meditech Co., Ltd. manufactures spinal bone screws, internal spinal fixation system rods and connectors, and non-bioabsorbable orthopaedic bone pins. The company also produces spinal implant trials, reusable bone taps, surgical screwdrivers, and orthopaedic counter-torque and rod-pushing instruments, as well as PEEK cervical and TL cages.

The company is based in the US, and its portfolio of Class I and Class II medical devices is listed in the FDA UDI database.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
687941818

Catalogue (6509)

Page 46 of 131
DeviceModel / ReferenceRegistriesClassStatus
Innesis Peek Cage 52780-11
FDA UDI
Class IActive
Mega5.5 Spine System 82130-110
FDA UDI
Class IIActive
Mega Plus Mis Spine System 98495-30
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69985-60
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69120-055
FDA UDI
Class IIActive
Mega Plus Mis Spine System 97575-45
FDA UDI
Class IIActive
Mega Plus Spine System 96405-40
FDA UDI
Class IIActive
Mega Plus Spine System 93470-45
FDA UDI
Class IIActive
Mega Plus Spine System 94550-20
FDA UDI
Class IIActive
Mega Plus Mis Spine System 97660-30
FDA UDI
Class IIActive
Mega Plus Spine System 96195-85
FDA UDI
Class IIActive
Mega Plus Mis Spine System 93950-55
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69550-25
FDA UDI
Class IIActive
Mega Plus Spine System 95295-100
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69750-30
FDA UDI
Class IIActive
Mega Plus Spine System 95285-40
FDA UDI
Class IIActive
Mega Plus Spine System 94405-75
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69560-45
FDA UDI
Class IIActive
Mega Plus Mis Spine System 98675-30
FDA UDI
Class IIActive
Mega Plus Mis Spine System 98650-45
FDA UDI
Class IIActive
Mega Plus Mis Spine System 97670-45
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69975-45
FDA UDI
Class IIActive
Mega Plus Mis Spine System 98755-35
FDA UDI
Class IIActive
Mega Plus Mis Spine System 97685-95
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69220-300
FDA UDI
Class IIActive
Mega Plus Mis Spine System 94975-40
FDA UDI
Class IIActive
Mega Plus Mis Spine System 93695-80
FDA UDI
Class IIActive
Mega Plus Spine System 95170-50
FDA UDI
Class IIActive
Mega Plus Spine System 96205-80
FDA UDI
Class IIActive
Mega Plus Spine System 96245-40
FDA UDI
Class IIActive
Mega Plus Mis Spine System 93705-35
FDA UDI
Class IIActive
Mega Plus Spine System 81107-07
FDA UDI
Class IIActive
Mega Plus Spine System 61321-190
FDA UDI
Class IIActive
Mega Plus Mis Spine System 97705-65
FDA UDI
Class IIActive
Mega Plus Spine System 82120-04H
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69230-250
FDA UDI
Class IIActive
Mega Plus Mis Spine System 94785-30
FDA UDI
Class IIActive
Mega Plus Spine System 95245-26
FDA UDI
Class IIActive
Mega Plus Spine System 95145-50
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69131-280
FDA UDI
Class IIActive
Mega Plus Spine System 96185-60
FDA UDI
Class IIActive
Mega Plus Mis Spine System 98170-50
FDA UDI
Class IIActive
Mega Plus Mis Spine System 97975-35
FDA UDI
Class IIActive
Mega Plus Spine System 93515-15
FDA UDI
Class IIActive
Mega Plus Spine System 94185-45
FDA UDI
Class IIActive
Mega Plus Mis Spine System 69220-120
FDA UDI
Class IIActive
Mega Plus Spine System 94130-41
FDA UDI
Class IIActive
Mega Plus Mis Spine System 94655-30
FDA UDI
Class IIActive
Mega Plus Mis Spine System 13100
FDA UDI
Class IActive
Mega Plus Spine System 11060
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Bk Meditech Co., Ltd. Hwaseong-si Gyeonggi · KR FEI 3004176895