Facility

NEOMED CO., LTD.

2 recall(s) on record — most severe on record: Class II.

Key facts

2recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3012865799
Establishment type	Manufacture Medical Device
Location	20, Jangnim-ro 196beon-gil Saha-gu Busan, KR 49475
Registration status	Active · expires 2026
Parent company	Neomed Co., Ltd. (owner-operator 10053119)
Brand names	JC-612 NEO NECK DELIGHT; JC- 7007 NEO NECK PLEASURE; JC-600 NEO NECK STRONG; JC-777 NEO MULTI COLLAR

Activity by year

Recalls (2)

Devices registered here (1)

Orthosis, Cervical
Product code IQK (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3490

Recalls & enforcement

Class IIITerminated2018-10-24
The sterile pouch label states the expiration date is 2016-11-19, but the correct expiration date is 2019-11-09. The case label and the shipper label have the correct date
Class IITerminated2018-06-04
Potential for the tethered plug on the hub of the NeoMed Enteral Feeding Tubes with Enteral Only Connectors to inadvertently open after closure.

All facilities operated by Neomed Co., Ltd.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “NEOMED CO., LTD. (FEI 3012865799) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3012865799-neomed-co-ltd/

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