Richline Group, Inc. D/b/a Inverness

The Inverness 2000 Ear Piercing Earring provides a means for safe and reliable ear piercing. The product includes a reusable or single Ear Piercing instrument which holds an integrated…

Registry build 21.09.26

The Inverness 2000 Ear Piercing Earring provides a means for safe and reliable ear piercing. The product includes a reusable or single Ear Piercing instrument which holds an integrated disposable cartridge. The integrated cartridge houses both a piercing earring within a disposable protective capsule and a fully enclosed safety clutch. Hand pressure activation of the instrument advances the capsule from the cartridge to the ear lobe. Further hand pressure advances the piercing posted earring from the capsule, through the ear and into a fully enclosed safety clutch. The earring is released from the capsule as the earring decorative element passes through and breaks the capsule retention webs. The clutch is released as the post tip displaces the clutch and a clutch retention finger. A lidded cassette houses and protects the sterility of two cartridges and contents prior to use.

2manufacturers in China registered for this device type
7catalogue numbers in this listing

Who Else Makes It

All of them in Jiangxi.

Chinese manufacturers registered for FDA product code JYS
Manufacturer City Province Registered as Device types
Jiujiang Meite Jewelry Co..Ltd. Jiujiang Jiangxi Manufacturer 3
Nanchang Firstomato Medical Devices Co., Ltd. Nanchang Jiangxi Manufacturer 1

Record

Regulatory record for Richline Group, Inc. d/b/a Inverness
Listed by Richline Group, Inc., United States
FDA product code JYS
Device type Perforator, Ear-Lobe
Device class Class 1
Regulation 21 CFR 874.4420
Establishment Specification developer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2026-02-26

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Richline Group, Inc. d/b/a Inverness
Catalogue number Size Status
Version 0 In distribution
Version 0 In distribution
Version 0 In distribution
version 0 In distribution
Version 0 In distribution
Version 0 In distribution
version 0 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Fisch footplate perforator Spiggle & Theis Medizintechnik Gmbh 6
Lucae tympanum perforator Spiggle & Theis Medizintechnik Gmbh 1
Bausch + Lomb Bausch & Lomb Incorporated 1
Richline Greoup, Inc. d/b/a Inverness Richline Group, Inc. 1
Politzer tympanum perforator Spiggle & Theis Medizintechnik Gmbh 1

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer